R62.52
BillableShort stature (child)
Short stature (child)
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Lack of growth
- Physical retardation
- Short stature NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Also Known As / Clinical Terms
SNOMED CT
- Inherited disorder of folate metabolism4702003
- Bilateral congenital dislocation of hip10155006
- Rachitic dwarf13109008
- Pelger-Huet cell15111002
- Pelger-Huët cell15111002
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Brachymetatarsia30592006
- Longitudinal deficiency of metatarsal bone30592006
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Blue sacral spot40467008
- Mongolian blue spot40467008
- Mongolian macula40467008
- Mongolian spot40467008
- Genetic anomaly of leucocyte47986005
- Genetic anomaly of leukocyte47986005
- Genetic leucocyte disorder47986005
- Genetic leukocyte disorder47986005
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Pentose disorder57507002
- Atresia of external auditory canal75355004
- Congenital atresia of external auditory canal75355004
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Pelger Huet anomaly85559002
- Pelger-Huet anomaly85559002
- Pelger-Huët anomaly85559002
- Advanced bone age123982003
- Delayed bone age123983008
- Retarded bone age123983008
- Abnormal blue sclerae204164000
- Blue sclera204164000
- Brachymesophalangia205317004
- Slow to talk229721007
- Speech delay229721007
- SS - Short stature237836003
- Short stature237836003
- Short stature disorder237836003
- Small stature237836003
- Livedo racemosa238772004
- Livedo reticularis238772004
- Hip pathological dislocation239759009
- CMTC - Cutis marmorata telangiectatica congenita254778000
- Congenital livedo reticularis254778000
- Cutis marmorata telangiectasia congenita254778000
- Cutis marmorata telangiectatica congenita254778000
- Van Lohuizen's syndrome254778000
- Blue naevus of skin254806009
- Blue nevus of skin254806009
- Has not grown in height271817008
- Height static271817008
- Lack of growth271817008
- Bone age finding397651006
- Cataract in child399336001
- Childhood cataract399336001
- Juvenile cataract399336001
- PIBIDS syndrome, photosensitivity with IBIDS403781006
- Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome403781006
- Short stature associated with bone marrow transplant429362002
- Short stature due to radiation therapy431038007
- Familial short stature432526008
- Genetic short stature432526008
- Retardation of physical development442168001
- Short stature for age444000005
- Growth retardation444896005
- Ear, patella, short stature syndrome703508009
- Meier-Gorlin syndrome703508009
- Microtia, absent patellae, micrognathia syndrome703508009
- Cataract with aberrant oral frenula and growth delay syndrome715988005
- Wellesley Carman French syndrome715988005
- Short stature with valvular heart disease and characteristic facies syndrome716193004
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- Trichothiodystrophy723551003
- Short stature of childhood735643002
- CHOPS syndrome764455002
- Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome764455002
- Chudley Rozdilsky syndrome764959000
- Intellectual disability, myopathy, short stature, endocrine defect syndrome764959000
- Congenital dislocation of left hip767002009
- Congenital dislocation of right hip767003004
- Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome771074000
- Intellectual disability, short stature, hypertelorism syndrome771077007
- Stoll Geraudel Chauvin syndrome771077007
- FILS (facial dysmorphism, immunodeficiency, livedo, short stature) syndrome771515001
- FILS syndrome771515001
- Facial dysmorphism, immunodeficiency, livedo, short stature syndrome771515001
- PSS - proportionate short stature772085001
- Proportionate short stature772085001
- DSS - disproportionate short stature772086000
- Disproportionate short stature772086000
- Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome773419004
- Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome773419004
- SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome773625007
- SOFT syndrome773625007
- Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome773625007
- SAMS (short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies) syndrome774155009
- SAMS syndrome774155009
- Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome774155009
- Brachymetatarsia of 4th metatarsal890191004
- Brachymetatarsia of fourth metatarsal890191004
- Abnormally short fourth metatarsal897459007
- Short fourth metatarsal897459007
- Lethal congenital SLSS (short limb short stature)926342004
- Lethal congenital disproportionate short limbed short stature926342004
- Lethal congenital short limb short stature926342004
- Lethal congenital STSS (short trunk short stature)926343009
- Lethal congenital disproportionate short trunk short stature926343009
- Lethal congenital short trunk short stature926343009
- Congenital dysplasia of nail unit1142193008
- Hypoplasia of distal phalanx of hand1145503000
- Short stature disorder due to osteosclerosis1153392009
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome1172605003
- Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome1172629005
- X-linked facial dysmorphism, short stature, choanal atresia, intellectual disability syndrome limited to females1172697000
- X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability1172697000
- OFD18 - oral-facial-digital syndrome type 181177179002
- Oral-facial-digital syndrome with short stature and brachymesophalangia1177179002
- Orofaciodigital syndrome type 181177179002
- Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome1186729007
- Microcephalic cortical malformations, short stature due to RTTN (rotatin) deficiency1187195007
- Microcephalic cortical malformations, short stature due to RTTN deficiency1187195007
- Microcephalic cortical malformations, short stature due to rotatin deficiency1187195007
- SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures1187277001
- Short stature, brachydactyly, obesity, global developmental delay syndrome1187277001
- Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome1187303004
- Short stature, advanced bone age, early-onset osteoarthritis syndrome1197586007
- Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome1197589000
- Steel syndrome1197589000
- Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome1208746001
- Psychosocial short stature1217076005
- Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome1217229007
- Developmental delay, short stature, dysmorphic features, sparse hair syndrome1217229007
- Loucks Innes syndrome1217229007
- Severe myopia, generalised joint laxity, short stature syndrome1217372003
- Severe myopia, generalized joint laxity, short stature syndrome1217372003
- Retinal dystrophy, juvenile cataract, short stature syndrome1220597000
- Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome1220597000
- Short stature, developmental delay, congenital heart defect syndrome1237512003
- TKT (transketolase) deficiency disorder1237512003
- Transketolase deficiency disorder1237512003
- SOPH (short stature, optic nerve atrophy, Pelger-Huët anomaly) syndrome1237618009
- Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome1237618009
- X-linked intellectual disability, short stature, overweight syndrome1255335006
- MTHFS (methenyltetrahydrofolate synthetase) related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- Diets Jongmans syndrome1351843001
- KDM3B-related intellectual disability, facial dysmorphism, short stature syndrome1351843001
- Lysine demethylase 3B-related intellectual disability, facial dysmorphism, short stature syndrome1351843001
- Genetic syndromic childhood obesity1359763002
- Body height below reference range1363478003
- Below expected growth rate440301000124106
- Below normal growth rate440301000124106
- Decreased growth rate440301000124106
- Suboptimal growth rate440301000124106
- Idiopathic short stature133221000119100
- Infantile and/or juvenile cataract342291000119102
- Pathological dislocation of bilateral hips15720721000119105
- Pathological dislocation of left hip15720681000119104
- Pathological dislocation of right hip15720761000119100
UMLS
- Decreased body heightC0349588
- Height less than 3rd percentileC0349588
- SS - Short statureC0349588
- Short StatureC0349588
- Short statureC0349588
- Short stature NOSC0349588
- Short stature:C0349588
- Small statureC0349588
- Stature below 3rd percentileC0349588
- Stature shortC0349588
- short statureC0349588
- small statureC0349588
- stature shortC0349588
- Lack of growthC1442754
- Physical retardationC0476243
- Short stature (child)C2830460
Frequently Asked Questions
What is the ICD-10 code for short stature (child)?
The ICD-10-CM code for short stature (child) is R62.52. The full clinical description is "Short stature (child)". R62.52 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code R62.52 mean?
ICD-10-CM code R62.52 represents "Short stature (child)". It is classified under Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings and is a billable/specific code that can be used on a claim.
Is R62.52 a billable code?
Yes, R62.52 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is R62.52 in?
R62.52 is in Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings (codes R00-R99).
What codes cannot be used with R62.52?
R62.52 has Excludes1 notes indicating codes that cannot be used together with it, including: delayed puberty (E30.0); gonadal dysgenesis (Q99.1); hypopituitarism (E23.0); and 3 more.
What SNOMED CT codes does R62.52 map to?
R62.52 maps to 87 SNOMED CT concepts: 204164000, 897459007, 123982003, 75355004, 440301000124106, and 82 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for R62.52?
R62.52 is linked to 4 UMLS Concept Unique Identifiers: C0349588, C1442754, C0476243, C2830460. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.