Height (SNOMED)

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Codelist metadata

Coding system

SNOMED CT

Coding system release

unknown

Organisation

OpenSAFELY

Codelist ID

opensafely/height-snomed

Version ID

3b4a3891

Versions

  • 3b4a3891 Updated: 2023-11-23 16:10:59

About

Description

Returns body height measurements.

Methodology

Used the search term "height" and included codes pertaining to body height.

References

Signed off by

  • Robin Park, (Feb. 3, 2022)
  • Caroline Morton, (Feb. 3, 2022)

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code term
139977008 O/E - height
14456009 Measuring height of patient
162755006 On examination - height
248327008 General finding of height
248333004 Standing height
50373000 Body height measure

Codes not in the full codelist are in faint grey.

This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.

height

Included 6 out of 631 matching concepts.

Show matching concepts
  • 12q14 microdeletion syndrome (719046005)
  • 21q22.11q22.12 microdeletion syndrome (787171006)
  • Aarskog syndrome (14921002)
  • Abdominal hyperesthesia (18156008)
  • Able to clean items at shoulder height (942711000000101)
  • Able to clean items at shoulder height (716400004)
  • Able to clean items at waist height (942721000000107)
  • Able to clean items at waist height (716401000)
  • Abnormal height in relation to growth / age standard (425115008)
  • Abnormal increase in body height (14811000119105)
  • Absent thumb with short stature and immunodeficiency syndrome (719685004)
  • Achondrogenesis (2391001)
  • Achondrogenesis, type IA (42725006)
  • Achondrogenesis, type IB (14870002)
  • Achondrogenesis, type II (254061001)
  • Achondroplasia (86268005)
  • Acromicric dysplasia (254090007)
  • Acroscyphodysplasia (389162001)
  • Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (733072002)
  • Allodynia (247404004)
  • Anterior face height (711582005)
  • Appropriate growth (224996000)
  • Arrested development following protein-calorie malnutrition (74257000)
  • Asexual dwarfism (7530009)
  • Ataxia, photosensitivity, short stature syndrome (773769008)
  • Ateleiotic dwarfism (71003000)
  • Autosomal dominant Robinow syndrome (890233009)
  • Autosomal dominant brachyolmia (717264003)
  • Autosomal recessive Robinow syndrome (890237005)
  • Autosomal recessive asexual dwarfism (17192009)
  • Autosomal recessive brachyolmia (783789002)
  • Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (716195006)
  • Autosomal recessive isolated somatotropin deficiency (18200000)
  • Baby length centile (281054006)
  • Beckwith-Wiedemann syndrome (81780002)
  • Below expected growth rate (440301000124106)
  • Biemond syndrome type 2 (717887003)
  • Bilateral Madelung deformity (890380004)
  • Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency (237614004)
  • Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (717914000)
  • Bloom syndrome (4434006)
  • Body growth problem (301329004)
  • Body height abnormal for age (129814003)
  • Body height growth rate (870593000)
  • Body height growth rate (1060601000000109)
  • Body height measure (50373000)
  • Body height measurement declined (1037511000000103)
  • Body height measurement declined (1037521000000109)
  • Body height normal for age (17489000)
  • Body position for height measurement (425260001)
  • Bone age corrected height centile (302033003)
  • Brachycephalic face (699783006)
  • Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (765761009)
  • Brachydactyly, short stature, retinitis pigmentosa syndrome (782914000)
  • Brachymorphism with onychodysplasia and dysphalangism syndrome (720573009)
  • Brachyolmia (254088006)
  • Brachyolmia - Maroteaux type (389165004)
  • Brachytelephalangy, facial dysmorphism, Kallmann syndrome (720574003)
  • Camptomelic dysplasia (74928006)
  • Carbohydrate sulfotransferase 3 related skeletal dysplasia (725417001)
  • Cardiospondylocarpofacial syndrome (720612000)
  • Carpenter Waziri syndrome (719101006)
  • Cataract with aberrant oral frenula and growth delay syndrome (715988005)
  • Caudal appendage deafness syndrome (726621009)
  • Child height 0.5th - 1.9th centile (147275000)
  • Child height 0.5th - 1.9th centile (170043000)
  • Child height 0.5th - 1.9th centile (314688005)
  • Child height 10th - 24th centile (314692003)
  • Child height 10th - 24th centile (170047004)
  • Child height 10th - 24th centile (147279006)
  • Child height 26th - 49th centile (314694002)
  • Child height 26th - 49th centile (170049001)
  • Child height 26th - 49th centile (147281008)
  • Child height 3rd - 8th centile (170045007)
  • Child height 3rd - 8th centile (147277008)
  • Child height 51st - 74th centile (314696000)
  • Child height 51st - 74th centile (147283006)
  • Child height 51st - 74th centile (170051002)
  • Child height 76th - 90th centile (147285004)
  • Child height 76th - 90th centile (170053004)
  • Child height 76th - 90th centile (314698004)
  • Child height 92nd - 97th centile (170055006)
  • Child height 92nd - 97th centile (314700008)
  • Child height 92nd - 97th centile (147287007)
  • Child height 98.1st - 99.6th centile (170057003)
  • Child height 98.1st - 99.6th centile (314702000)
  • Child height 98.1st - 99.6th centile (147289005)
  • Child height < 0.4th centile (170042005)
  • Child height < 0.4th centile (147274001)
  • Child height < 0.4th centile (314687000)
  • Child height = 0.4th centile (147291002)
  • Child height = 0.4th centile (314756007)
  • Child height = 0.4th centile (170059000)
  • Child height = 25th centile (314693008)
  • Child height = 25th centile (170048009)
  • Child height = 25th centile (147280009)
  • Child height = 2nd centile (314689002)
  • Child height = 2nd centile (147276004)
  • Child height = 2nd centile (170044006)
  • Child height = 50th centile (314695001)
  • Child height = 50th centile (147282001)
  • Child height = 50th centile (170050001)
  • Child height = 75th centile (170052009)
  • Child height = 75th centile (147284000)
  • Child height = 75th centile (314697009)
  • Child height = 91st centile (147286003)
  • Child height = 91st centile (314699007)
  • Child height = 91st centile (170054005)
  • Child height = 98th centile (147288002)
  • Child height = 98th centile (314701007)
  • Child height = 98th centile (170056007)
  • Child height = 9th centile (170046008)
  • Child height = 9th centile (147278003)
  • Child height = 9th centile (314691005)
  • Child height > 99.6th centile (147290001)
  • Child height > 99.6th centile (314703005)
  • Child height > 99.6th centile (170058008)
  • Child height centile (268482007)
  • Child height centile finding (365889005)
  • Child height centiles (& [baby length]) (147265003)
  • Child height centiles (& [baby length]) (170033003)
  • Child height centiles NOS (147292009)
  • Child height centiles NOS (170060005)
  • Child height centiles NOS (554511000000106)
  • Child height equal to third-ninth centile (170035005)
  • Child height greater than 97th centile (170041003)
  • Child height greater than 97th centile (147273007)
  • Child height less than third centile (170034009)
  • Child height less than third centile (147266002)
  • Child height third - eighth centile (314690006)
  • Child height=10th-24th centile (147268001)
  • Child height=10th-24th centile (170036006)
  • Child height=25th-49th centile (170037002)
  • Child height=25th-49th centile (147269009)
  • Child height=3rd-9th centile (147267006)
  • Child height=50th-74th centile (170038007)
  • Child height=50th-74th centile (147270005)
  • Child height=75th-89th centile (170039004)
  • Child height=75th=89th centile (147271009)
  • Child height=90th-96th centile (147272002)
  • Child height=90th-96th centile (170040002)
  • Chondrodysplasia with disorder of sex development syndrome (720851007)
  • Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (717823001)
  • Cleft palate with short stature and vertebral anomaly syndrome (719466009)
  • Cleft palate, large ears, small head syndrome (763130006)
  • Cleidorhizomelic syndrome (719471002)
  • Colobomatous microphthalmia, rhizomelic dysplasia syndrome (764942005)
  • Congenital cataract, nephropathy, encephalopathy syndrome (722381004)
  • Congenital malformation syndromes associated with short stature (205808005)
  • Cono-spondylar dysplasia (766874001)
  • Constitutional short stature (422065006)
  • Constitutional tall stature (237835004)
  • Coxoauricular syndrome (732248005)
  • Craniofaciofrontodigital syndrome (763320005)
  • Craniolenticulosutural dysplasia (725100001)
  • Crown heel length (276353004)
  • Cutaneous allodynia (403597003)
  • Cutaneous hyperalgesia (403596007)
  • Cutaneous mastocytosis, short stature, hearing loss syndrome (722453009)
  • Czech dysplasia metatarsal type (720826006)
  • De Lange syndrome (40354009)
  • Deafness, vitiligo, achalasia syndrome (733069009)
  • Decrease in height (71781005)
  • Decreased body growth (102494001)
  • Decreased lower anterior face height (711466007)
  • Decreased lower face height (711461002)
  • Decreased posterior face height (711463004)
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (721089006)
  • Developmental height centile is cause for concern (300031000000108)
  • Diastrophic dysplasia (58561002)
  • Difficulty cleaning items at shoulder height (1069911000000106)
  • Difficulty cleaning items at waist height (1069921000000100)
  • Disorder of stature (237834000)
  • Disproportionate short stature (772086000)
  • Distal arthrogryposis type 3 (897570002)
  • Distribution pattern of hair growth (247534007)
  • Does clean items at shoulder height (1073201000000108)
  • Does clean items at waist height (1073211000000105)
  • Does not clean items at shoulder height (1071531000000101)
  • Does not clean items at waist height (1071541000000105)
  • Dolichocephalic dwarfism (39401000)
  • Down syndrome height centile (926081000000108)
  • Down's syndrome height centile (926091000000105)
  • Dubowitz's syndrome (2593002)
  • Dwarfism, alopecia, pseudoanodontia, cutis laxa (239025003)
  • Dyggve-Melchior-Clausen syndrome (82699004)
  • Dyschondrosteosis and nephritis syndrome (722433005)
  • Dysmorphism, short stature, deafness, disorder of sex development syndrome (733050004)
  • Dyssegmental dysplasia Silverman Handmaker type (765204000)
  • Ear, patella, short stature syndrome (703508009)
  • Eiken syndrome (720863002)
  • Electrocardiographic complex height (251219003)
  • Emery Nelson syndrome (773768000)
  • Epiphyseal dysplasia, microcephalus, nystagmus syndrome (721975004)
  • Eunuchoid gigantism (2041006)
  • Evaluation of uterine fundal height (274804006)
  • Excessive growth rate (440311000124109)
  • Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (771179007)
  • Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (771515001)
  • Fall from height (240811000000109)
  • Fall from high place (429482004)
  • Fall through height of between one and two metres (240861000000106)
  • Fall through height of less than one metre (240871000000104)
  • Fall through height of more than five metres (240881000000102)
  • Fall through height of more than two and less than five metres (240891000000100)
  • Faltering growth rate (909661000000108)
  • Familial infantile gigantism (773645004)
  • Familial short stature (432526008)
  • Fear of heights (276241001)
  • Feeding environment table height management (444581000124104)
  • Finding of bone height of edentulous mandible (710083001)
  • Finding of fetal growth (289447005)
  • Finding of fundal height of uterus (289625003)
  • Finding of height of gravid uterus (289682002)
  • Finding of measures of body height and growth (301330009)
  • Fitting point height (397257003)
  • Floating-Harbor syndrome (312214005)
  • Fundal height equal to dates (289684001)
  • Fundal height high for dates (289683007)
  • Fundal height low for dates (289685000)
  • Fundal height of uterus (364253002)
  • Furniture height modification (228626002)
  • Furniture height-adjustment assistive device (705393006)
  • Geleophysic dysplasia (28557005)
  • General finding of height (248327008)
  • General growth finding (248330001)
  • Gigantism (80849007)
  • Gigantism and acromegaly (267386008)
  • Gigantism due to somatostatin deficiency (12331003)
  • Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (722450007)
  • Goniodysgenesis with intellectual disability and short stature syndrome (716024001)
  • Growth delay due to insulin-like growth factor I resistance (715625007)
  • Growth hormone receptor abnormality (237839005)
  • Growth hormone receptor absent (237838002)
  • Growth pattern (404963005)
  • Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (721843003)
  • Growth velocity centile (248340003)
  • Guardrail height (18779001)
  • Hallermann-Streiff syndrome (7903009)
  • Has grown in height (248331002)
  • Has grown shorter (248329006)
  • Has not grown in height (271817008)
  • Heel height of footwear (963921000000106)
  • Heel height of footwear (939481000000107)
  • Heel height of footwear (716540007)
  • Height / growth finding (365714001)
  • Height / growth measure (271603002)
  • Height above average (418317006)
  • Height and Weight (140096001)
  • Height and weight (162879003)
  • Height and weight measurement for National Child Measurement Programme (758931000000104)
  • Height below average (418519005)
  • Height centile (248338008)
  • Height from demispan (248337003)
  • Height increased (224997009)
  • Height of alveolar bone surrounding teeth (769045007)
  • Height of alveolar bone surrounding tooth (769046008)
  • Height of crown of tooth (110311009)
  • Height of gravid uterus (364265003)
  • Height of palpebral fissure (246794004)
  • Height of skull (248378001)
  • Height of tumor at cut edge, after sectioning (396947001)
  • Height of upper lid above pupil center (246793005)
  • Height of uterine fundus (249016007)
  • Height of uterine fundus (856381000000103)
  • Height simple reference set (999000791000000105)
  • Height-adjustable chassis assistive automobile (469912003)
  • Heightened (260365005)
  • Heightened auditory perception (247713003)
  • Heightened erotic interest (248094001)
  • Heightened global phobia (110358001)
  • Heightened olfactory perception (247720005)
  • Heightened perception (247712008)
  • Heightened perception of taste (247722002)
  • Heightened sensation of skin (247327006)
  • Heightened tactile perception (247721009)
  • Heightened visual perception (247716006)
  • Hemoglobin Boyle Heights (65288007)
  • Hip dysplasia Beukes type (721148005)
  • Hydrocephalus, tall stature, joint laxity syndrome (732926009)
  • Hyperacusis (25289003)
  • Hyperacusis of bilateral ears (1083821000119101)
  • Hyperacusis of left ear (1088941000119107)
  • Hyperacusis of right ear (1091551000119105)
  • Hyperalgesia (55406008)
  • Hyperesthesia (14151009)
  • Hyperesthesia dolorosa (26857005)
  • Hyperesthesia of special senses (289174003)
  • Hypergargalesthesia (719048006)
  • Hypersomatotropic gigantism (86073008)
  • Hypochondroplasia (205468002)
  • Hypogonadism with mitral valve prolapse and intellectual disability syndrome (721841001)
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (773665006)
  • Hypothyroid dwarfism (216693007)
  • Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (733097003)
  • Ichthyosis, short stature, brachydactyly, microspherophakia syndrome (783551005)
  • Idiopathic short stature (133221000119100)
  • Immuno-osseous dysplasia (254067002)
  • Inadequate growth rate (906341000000109)
  • Increased body growth (102493007)
  • Increased lower anterior face height (711465006)
  • Increased lower face height (711460001)
  • Increased posterior face height (710780005)
  • Infant length (276351002)
  • Infantile dwarf (21265004)
  • Injury of unknown intent due to fall from bridge (242980007)
  • Injury of unknown intent due to fall from height (219346009)
  • Injury of unknown intent due to fall from high building (242978001)
  • Injury of unknown intent due to fall from high man-made structure (242977006)
  • Injury of unknown intent due to fall from high natural feature (242981006)
  • Injury of unknown intent due to fall off cliff (242982004)
  • Injury undetermined whether accidentally or purposely inflicted, fall from natural site (219349002)
  • Injury undetermined whether accidentally or purposely inflicted, fall from residential premises (219347000)
  • Insufficient anatomic crown height (110312002)
  • Insufficient clinical crown height (110313007)
  • Insufficient clinical crown height due to altered passive eruption (110314001)
  • Insufficient clinical crown height due to dental caries (110315000)
  • Insufficient clinical crown height due to fracture (110316004)
  • Intellectual disability and short stature with hand contracture and genital anomaly syndrome (716334004)
  • Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (773552008)
  • Intellectual disability, myopathy, short stature, endocrine defect syndrome (764959000)
  • Intellectual disability, short stature, hypertelorism syndrome (771077007)
  • Intermediate segment height (418423000)
  • Jumping from bridge (225046007)
  • Jumping from building (225047003)
  • Jumping from cliff (224950008)
  • Jumping from height (225048008)
  • Kabuki make-up syndrome (313426007)
  • Keratosis follicularis, dwarfism, cerebral atrophy syndrome (723830005)
  • Knee height (340781000000100)
  • Knee height (404924003)
  • Langer mesomelic dysplasia syndrome (38494008)
  • Laron syndrome with immunodeficiency (724179008)
  • Laron-type isolated somatotropin defect (38196001)
  • Larsen-like osseous dysplasia, short stature syndrome (764956007)
  • Length of body (248334005)
  • Leprechaunism syndrome (111307005)
  • Leri-Weill dyschondrosteosis (17818006)
  • Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (719405005)
  • Linear growth of stature completed (370978001)
  • Long face height (711584006)
  • Lower anterior face height (711464005)
  • Lower face height (711459006)
  • Macrocephaly, short stature, paraplegia syndrome (722033000)
  • Madelung's deformity (4530000)
  • Marfanoid habitus, inguinal hernia, advanced bone age syndrome (782780007)
  • Marginal ridge height discrepancy (697931003)
  • Maroteaux-Lamy syndrome (69463008)
  • Maroteaux-Lamy syndrome, intermediate form (26015003)
  • Maroteaux-Lamy syndrome, mild form (67854007)
  • Maroteaux-Lamy syndrome, severe form (58263000)
  • Mauriac's syndrome (80660001)
  • Maximal height of tumor, after sectioning (396948006)
  • Measuring height of patient (14456009)
  • Mesomelic dysplasia (205473008)
  • Mesomelic dysplasia Kantaputra type (719397009)
  • Mesomelic dysplasia Savarirayan type (715652002)
  • Mesomelic dysplasia of hypoplastic ulna and fibula type (715472000)
  • Mesomelic dysplasia of upper limb (1010609002)
  • Mesomelic dysplasia with cleft palate and camptodactyly syndrome (715471007)
  • Metaphyseal anadysplasia (254085009)
  • Metaphyseal chondrodysplasia (28681006)
  • Metaphyseal chondrodysplasia Kaitila type (770909004)
  • Metaphyseal chondrodysplasia, Jansen type (24629003)
  • Metaphyseal chondrodysplasia, McKusick type (7720002)
  • Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (304576008)
  • Metaphyseal chondrodysplasia, Schmid type (29248006)
  • Metaphyseal chondrodysplasia, Sedaghatian type (389163006)
  • Metaphyseal chondrodysplasia, Spahr type (254084008)
  • Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (733419006)
  • Metatropic dysplasia (22764001)
  • Method for measuring height (422769007)
  • Microcephalic osteodysplastic dysplasia Saul Wilson type (723404002)
  • Microcephalic osteodysplastic primordial dwarfism types I and III (725461009)
  • Microcephalic primordial dwarfism Alazami type (770564004)
  • Microcephalic primordial dwarfism Dauber type (770565003)
  • Microcephalic primordial dwarfism Montreal type (765758008)
  • Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency (724141003)
  • Microcephalic primordial dwarfism of Toriello type (715482004)
  • Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type (719395001)
  • Microcephalus with brachydactyly and kyphoscoliosis syndrome (719378009)
  • Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (733092009)
  • Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (771074000)
  • Microspherophakia with metaphyseal dysplasia syndrome (724140002)
  • Mid-parental centile (925971000000101)
  • Mid-parental height (925931000000103)
  • Mid-parental height (925941000000107)
  • Moderate nutritional stunting in infancy childhood and adolescence (717929003)
  • Monitoring height (710996002)
  • Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (724097003)
  • Multiple epiphyseal dysplasia (59708000)
  • Multiple epiphyseal dysplasia Al-Gazali type (719688002)
  • Multiple epiphyseal dysplasia Beighton type (719689005)
  • Multiple epiphyseal dysplasia Lowry type (768935003)
  • Multiple epiphyseal dysplasia due to collagen 9 anomaly (766717008)
  • Multiple epiphyseal dysplasia tarda type IIIa (313339007)
  • Multiple epiphyseal dysplasia type 1 (715673002)
  • Multiple epiphyseal dysplasia type 4 (715672007)
  • Multiple epiphyseal dysplasia type 5 (715674008)
  • Multiple epiphyseal dysplasia with miniepiphyses (766750008)
  • Multiple epiphyseal dysplasia with severe proximal femoral dysplasia (763893008)
  • Multiple malformation syndrome, small stature, without skeletal dysplasia (41483000)
  • Myhre syndrome (699316006)
  • Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome (764995008)
  • Namaqualand hip dysplasia (254064009)
  • Nievergelt's syndrome (33979003)
  • Nijmegen breakage syndrome-like disorder (766753005)
  • Nonfamilial asexual dwarfism (20900005)
  • Normal fetal growth (181833004)
  • Normal growth (58236001)
  • Normal height (309534003)
  • Not aware of danger from falling from heights (248082005)
  • Nutritional stunting (302869005)
  • Nutritional stunting in adolescence (762501002)
  • Nutritional stunting in childhood (762500001)
  • Nutritional stunting in infancy (762499005)
  • O/E - height (139977008)
  • O/E - height 10-20% below average (139979006)
  • O/E - height NOS (139984000)
  • O/E - height greater than 20% below average (139978003)
  • O/E - height greater than 20% over average (139982001)
  • O/E - loss of height (139983006)
  • O/E -height within 10% average (139980009)
  • O/E-height 10-20% over average (139981008)
  • Oculomaxillofacial dysostosis (763830009)
  • On examination - height (162755006)
  • On examination - height 10-20% below average (162757003)
  • On examination - height 10-20% over average (162759000)
  • On examination - height NOS (594151000000105)
  • On examination - height NOS (162762002)
  • On examination - height greater than 20% below average (162756007)
  • On examination - height greater than 20% over average (162760005)
  • On examination - height within 10% average (162758008)
  • On examination - loss of height (162761009)
  • Opsismodysplasia (254068007)
  • Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (722108000)
  • Osteodysplastic primordial dwarfism (254101001)
  • Osteodysplastic primordial dwarfism, type 1 (254102008)
  • Osteodysplastic primordial dwarfism, type 2 (254103003)
  • Osteogenesis imperfecta type 5 (1003379004)
  • Otospondylomegaepiphyseal dysplasia (254060000)
  • P wave height (251220009)
  • Parastremmatic dwarfism (722210007)
  • Patient-height measure (462588003)
  • Patterns appear interesting (247719004)
  • Patterns appear intricately detailed (247718007)
  • Pectus excavatum, macrocephaly, dysplastic nails syndrome (763863002)
  • Physical growth is cause for concern (302111000000100)
  • Physical retardation due to protein-calorie malnutrition (267410008)
  • Pituitary dwarfism (367460001)
  • Pituitary dwarfism with large sella turcica (27270004)
  • Pituitary dwarfism with normal somatotropin level AND low somatomedin (51371005)
  • Pituitary dwarfism with small sella turcica (91187007)
  • Poor clinical fetal growth (277658006)
  • Port-wine stain in Rubinstein-Taybi syndrome (403765001)
  • Posterior face height (711462009)
  • Predicted adult height (925951000000105)
  • Predicted adult height (925961000000108)
  • Primary immunodeficiency syndrome due to p14 deficiency (718717004)
  • Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (782755007)
  • Primordial dwarfism (237837007)
  • Progressive pseudorheumatoid dysplasia (254065005)
  • Proportionate short stature (772085001)
  • Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome (22567005)
  • Pseudoleprechaunism syndrome Patterson type (771262009)
  • Pubis to ground height (248336007)
  • Q wave height (251224000)
  • Q wave height decreased (251226003)
  • Q wave height increased (251225004)
  • QRS complex height (251233003)
  • QRS complex height decreased (251235005)
  • QRS complex height increased (251234009)
  • R wave height (251227007)
  • R wave height decreased (251229005)
  • R wave height increased (251228002)
  • Rachitic dwarf (13109008)
  • Radioulnar synostosis with microcephaly and scoliosis syndrome (719162001)
  • Ratio of upper to lower face height (251300005)
  • Reading segment height (419309008)
  • Record of fundal height measurement (820141000000107)
  • Renal dwarfism (36914006)
  • Reunion Island Larsen-like syndrome (783559007)
  • Rhizomelic syndrome Urbach type (770948004)
  • Richieri Costa-da Silva syndrome (782941005)
  • Robinow syndrome (76520005)
  • Roifman syndrome (773404000)
  • Rolland-Debuqois syndrome (95243004)
  • Rubinstein-Taybi syndrome (45582004)
  • Rud's syndrome (2355008)
  • Russell-Silver syndrome (15069006)
  • S wave height (251230000)
  • S wave height decreased (251232008)
  • S wave height increased (251231001)
  • Schimke immuno-osseous dysplasia (723995003)
  • Schneckenbecken dysplasia (254049009)
  • Seckel syndrome (57917004)
  • Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (874931001)
  • Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (773419004)
  • Severe lateral tibial bowing with short stature (766819001)
  • Severe nutritional stunting in infancy childhood and adolescence (717930008)
  • Sexual preoccupation (247635000)
  • Short stature Brussels type (719213009)
  • Short stature associated with bone marrow transplant (429362002)
  • Short stature co-occurrent and due to endocrine disorder (368331000119100)
  • Short stature disorder (237836003)
  • Short stature due to growth hormone secretagogue receptor deficiency (766817004)
  • Short stature due to partial growth hormone receptor deficiency (783098009)
  • Short stature due to primary acid labile subunit deficiency (721074002)
  • Short stature due to radiation therapy (431038007)
  • Short stature for age (444000005)
  • Short stature homeobox related short stature (763868006)
  • Short stature locking fingers syndrome (726734001)
  • Short stature of childhood (735643002)
  • Short stature with craniofacial anomalies and genital hypoplasia syndrome (716090004)
  • Short stature with delayed bone age due to thyroid hormone metabolism deficiency (763890006)
  • Short stature with webbed neck and congenital heart disease syndrome (721073008)
  • Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome (774155009)
  • Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (773625007)
  • Short stature, pituitary and cerebellar defect and small sella turcica syndrome (721072003)
  • Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (726672000)
  • Short stature, wormian bones, dextrocardia syndrome (763631006)
  • Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome (711156009)
  • Shwachman syndrome (89454001)
  • Sitting height (248335006)
  • Skeletal dysplasia with epilepsy and short stature syndrome (715428003)
  • Smith Fineman Myers syndrome (719212004)
  • Smith McCort dysplasia (715862006)
  • Sotos' syndrome (75968004)
  • Sounds seem unnaturally clear (247714009)
  • Sponastrime dysplasia (389161008)
  • Spondylo-megaepiphyseal-metaphyseal dysplasia (773693005)
  • Spondyloenchondrodysplasia (254079002)
  • Spondyloenchondrodysplasia with immune dysregulation (703523004)
  • Spondyloepimetaphyseal disorder (254062008)
  • Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type (719172003)
  • Spondyloepimetaphyseal dysplasia Genevieve type (773303005)
  • Spondyloepimetaphyseal dysplasia Handigodu type (763885008)
  • Spondyloepimetaphyseal dysplasia Irapa type (717330004)
  • Spondyloepimetaphyseal dysplasia Isidor type (782821004)
  • Spondyloepimetaphyseal dysplasia Missouri type (719171005)
  • Spondyloepimetaphyseal dysplasia Shohat type (719201004)
  • Spondyloepimetaphyseal dysplasia aggrecan type (719165004)
  • Spondyloepimetaphyseal dysplasia anauxetic type (764460003)
  • Spondyloepimetaphyseal dysplasia matrilin-3 type (719166003)
  • Spondyloepimetaphyseal dysplasia with multiple dislocations (766820007)
  • Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome (773302000)
  • Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome (773300008)
  • Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (766821006)
  • Spondyloepiphyseal dysplasia Reardon type (718764004)
  • Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome (718765003)
  • Spondyloepiphyseal dysplasia tarda (51952004)
  • Spondyloepiphyseal dysplasia tarda Kohn type (719202006)
  • Spondyloepiphyseal dysplasia with congenital joint dislocations (702400006)
  • Standing height (248333004)
  • Step height (250001007)
  • Subaortic stenosis and short stature syndrome (783096008)
  • Subischial leg length (276350001)
  • Suicide or self injury by jumping from a height (219155000)
  • T wave height (251236006)
  • Tall for age (83077003)
  • Tall stature (248328003)
  • Tall stature, intellectual disability, facial dysmorphism syndrome (768843007)
  • Tear meniscus height (424544008)
  • Teletherapy height above couch (228826000)
  • Teletherapy pin height (228825001)
  • Terrified (225634009)
  • Thanatophoric dysplasia (29352008)
  • Thanatophoric dysplasia, type 1 (389157002)
  • Thanatophoric dysplasia, type 2 (389158007)
  • Things appear vividly colored (247717002)
  • Thoracic dysplasia and hydrocephalus syndrome (782951006)
  • Thoracomelic dysplasia (783003009)
  • Thumb deformity, alopecia, pigmentation anomaly syndrome (771182002)
  • Trend in height centile (248339000)
  • Trichomegaly with retina pigmentary degeneration and dwarfism syndrome (719944006)
  • Trigonocephaly, short stature, developmental delay syndrome (733066002)
  • Tryptophanuria with dwarfism (12045002)
  • Type I bone height of edentulous mandible (710084007)
  • Type II bone height of edentulous mandible (710085008)
  • Type III bone height of edentulous mandible (710086009)
  • Type IV bone height of edentulous mandible (710087000)
  • U wave height (251239004)
  • Ulna metaphyseal dysplasia syndrome (715242008)
  • Unsuitable for body height measurement (1046331000000104)
  • Unsuitable for body height measurement (1046341000000108)
  • Upper anterior face height (711583000)
  • Upper limb neurodynamic test 1 median nerve heightened mechanosensitivity detected (1103361000000102)
  • Upper limb neurodynamic test 1 median nerve heightened mechanosensitivity not detected (1103371000000109)
  • Upper limb neurodynamic test 2A median nerve heightened mechanosensitivity detected (1103381000000106)
  • Upper limb neurodynamic test 2A median nerve heightened mechanosensitivity not detected (1103391000000108)
  • Upper limb neurodynamic test 2B radial nerve heightened mechanosensitivity detected (1103401000000106)
  • Upper limb neurodynamic test 2B radial nerve heightened mechanosensitivity not detected (1103411000000108)
  • Upper limb neurodynamic test 3 ulnar nerve heightened mechanosensitivity detected (1103421000000102)
  • Upper limb neurodynamic test 3 ulnar nerve heightened mechanosensitivity not detected (1103431000000100)
  • Upper limb neurodynamic test of musculocutaneous nerve heightened mechanosensitivity detected (1103441000000109)
  • Upper limb neurodynamic test of musculocutaneous nerve heightened mechanosensitivity not detected (1103451000000107)
  • Uterine fundus above umbilicus (289629009)
  • Uterine fundus at symphysis pubis (289626002)
  • Uterine fundus at umbilicus (289627006)
  • Uterine fundus at xiphisternum (289631000)
  • Uterine fundus between symphysis pubis and umbilicus (289628001)
  • Uterine fundus between umbilicus and xiphisternum (289630004)
  • Velofacioskeletal syndrome (763616002)
  • Vertical vertigo (103288004)
  • Waist to height ratio (845541000000105)
  • Waist to height ratio (845551000000108)
  • Warsaw breakage syndrome (702829000)
  • Waterlow build/weight for height score (206061000000106)
  • Waterlow build/weight for height score (917251000000100)
  • Weight for height (248358009)
  • Weight for height (248360006)
  • Werner syndrome (51626007)
  • Wiedemann Steiner syndrome (763618001)
  • Wolcott-Rallison dysplasia (254066006)
  • X-linked acrogigantism due to Xq26 microduplication (789187001)
  • X-linked asexual dwarfism (57536002)
  • X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (771148008)
  • X-linked intellectual disability Atkin type (718577005)
  • X-linked intellectual disability Cilliers type (719013004)
  • X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (765471005)
  • X-linked spondyloepimetaphyseal dysplasia (770603000)
  • pT1: Tumor 10 mm or less in greatest diameter and 2.5 mm or less in greatest height (thickness) (ciliary body and choroid) (uveal melanoma) (399448002)
  • pT1a: Tumor 10 mm or less in greatest diameter and 2.5 mm or less in greatest height (thickness) without microscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399516003)
  • pT1b: Tumor 10 mm or less in greatest diameter and 2.5 mm or less in greatest height (thickness) with microscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399461002)
  • pT1c: Tumor 10 mm or less in greatest diameter and 2.5 mm or less in greatest height (thickness) with macroscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399493005)
  • pT2: Tumor greater than 10 mm but not more than 16 mm in greatest basal diameter and between 2.5 and 10 mm in maximum height (thickness) (ciliary body and choroid) (uveal melanoma) (399397007)
  • pT2a: Tumor 10 mm to 16 mm in greatest basal diameter and between 2.5 and 10 mm in maximum height (thickness) without microscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399519005)
  • pT2b: Tumor 10 mm to 16 mm in greatest basal diameter and between 2.5 and 10 mm in maximum height (thickness) with microscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399616006)
  • pT2c: Tumor 10 mm to 16 mm in greatest basal diameter and between 2.5 and 10 mm in maximum height (thickness) with macroscopic extraocular extension (ciliary body and choroid) (uveal melanoma) (399543008)
  • pT3: Tumor more than 16 mm in greatest diameter and/or greater than 10 mm in maximum height (thickness) without extraocular extension (ciliary body and choroid) (uveal melanoma) (399610000)
  • pT4: Tumor more than 16 mm in greatest diameter and/or greater than 10 mm in maximum height (thickness) with extraocular extension (ciliary body and choroid) (uveal melanoma) (399729000)