Diagnosis Code: R62.52

Short Description: Short stature (child)

Long Description: Short stature (child)

The code R62.52 is VALID for claim submission

Code Classification:

• Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00–R99)
  • General symptoms and signs (R50-R69)
    • Lack of expected normal physiol dev in childhood and adults (R62)
      • R62.52 Short stature (child)

Code Version: 2022 ICD-10-CM

Synonyms

• Abnormal blue sclerae
• Advanced bone age
• Below expected growth rate
• Bilateral congenital dislocation of hip
• Blue nevus of skin
• Bone age finding
• Bone age finding
• Brachydactyly of hand
• Brachymesophalangia
• Brachymetatarsia
• Brachymetatarsia of fourth metatarsal
• Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
• Congenital anomaly of sclera
• Congenital atresia of external auditory canal
• Congenital atrophy of optic nerve
• Congenital dislocation of left hip
• Congenital dislocation of right hip
• Congenital hypotrichia
• Congenital livedo reticularis
• Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome
• Delayed bone age
• Disproportionate short stature
• Ear, patella, short stature syndrome
• Facial dysmorphism, immunodeficiency, livedo, short stature syndrome
• Familial short stature
• Genetic anomaly of leukocyte
• Growth retardation
• Has not grown in height
• Height below average
• Hip pathological dislocation
• Hypertelorism
• Idiopathic short stature
• Infantile and/or juvenile cataract
• Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome
• Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome
• Intellectual disability, myopathy, short stature, endocrine defect syndrome
• Intellectual disability, short stature, hypertelorism syndrome
• Juvenile cataract
• Livedo reticularis
• Microcephalic cortical malformations, short stature due to RTTN deficiency
• Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome
• Mongolian spot
• Multiple malformation syndrome, moderate short stature, facial
• Oral-facial-digital syndrome with short stature and brachymesophalangia
• Pathological dislocation of left hip
• Pelger-Huët anomaly
• Pelger-Huët cell
• Pentose disorder
• Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
• Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome
• Proportionate short stature
• Psychosocial short stature
• Rachitic dwarf
• Retardation of physical development
• Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
• Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome
• Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome
• Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome
• Severe myopia, generalized joint laxity, short stature syndrome
• Short stature associated with bone marrow transplant
• Short stature disorder
• Short stature disorder due to osteosclerosis
• Short stature due to radiation therapy
• Short stature for age
• Short stature of childhood
• Short stature with valvular heart disease and characteristic facies syndrome
• Short stature, advanced bone age, early-onset osteoarthritis syndrome
• Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
• Short stature, brachydactyly, obesity, global developmental delay syndrome
• Short stature, developmental delay, congenital heart defect syndrome
• Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
• Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome
• Speech delay
• Steel syndrome
• Trichothiodystrophy
• Wellesley Carman French syndrome
• X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability
• X-linked intellectual disability, short stature, overweight syndrome

Diagnostic Related Group(s)

The code R62.52 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Miscellaneous Disorders Of Nutrition, Metabolism, Fluids And Electrolytes With Mcc (640)
• Miscellaneous Disorders Of Nutrition, Metabolism, Fluids And Electrolytes Without Mcc (641)

References to Index of Diseases and Injuries

The code R62.52 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Lack of growth
  • Physical retardation
  • Short stature NOS
• Type 1 Excludes Notes:
  • short stature due to endocrine disorder (@E34.3*-)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

« Previous Code