Diagnosis Code: Q87.19

Short Description: Other congen malform synd predom assoc with short stature

Long Description: Other congenital malformation syndromes predominantly associated with short stature

The code Q87.19 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Oth congenital malform syndromes affecting multiple systems (Q87)
      • Q87.19 Other congen malform synd predom assoc with short stature

Code Version: 2022 ICD-10-CM

Synonyms

• 6q16 microdeletion syndrome
• Aarskog syndrome
• Absent thumb with short stature and immunodeficiency syndrome
• Alopecia, contracture, dwarfism, intellectual disability syndrome
• Anterior pituitary hormone deficiency
• Ataxia, photosensitivity, short stature syndrome
• Atkin Flaitz syndrome
• Autosomal dominant Robinow syndrome
• Autosomal recessive Robinow syndrome
• Bent bone dysplasia group
• BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
• Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
• Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
• Bowing deformity of lower leg
• Brachydactyly, short stature, retinitis pigmentosa syndrome
• Brachymorphism with onychodysplasia and dysphalangism syndrome
• Chitty Hall Baraitser syndrome
• Chronic deafness
• Cleft mandible
• Cleft palate with short stature and vertebral anomaly syndrome
• Cockayne syndrome
• Cockayne syndrome
• Cockayne syndrome type 1
• Cockayne syndrome type 2
• Cockayne syndrome type 3
• Colobomatous microphthalmia
• Congenital abnormal shape of frontal bone
• Congenital abnormal shape of tibia
• Congenital absence of thumb
• Congenital blepharophimosis
• Congenital bowing of tibia and/or fibula
• Congenital hypoplasia of cerebrum
• Congenital leg bone bowing
• Congenital malformation of angle of anterior chamber of eye
• Congenital malformation of anterior pituitary
• Congenital malformation syndromes associated with short stature
• Congenital subaortic stenosis
• Coxoauricular syndrome
• Cutaneous mastocytosis
• Cutaneous syndrome with ichthyosis
• Dandy-Walker syndrome
• De Lange syndrome
• Defect of vertebral segmentation
• Deletion of part of chromosome 6
• Deletion of part of long arm of chromosome 6
• Dentinogenesis imperfecta
• Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
• Disturbance of hair cycle
• Dubowitz's syndrome
• Dwarfism, alopecia, pseudoanodontia, cutis laxa
• Dysmorphism, short stature, deafness, disorder of sex development syndrome
• Dyssegmental dysplasia Silverman Handmaker type
• Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
• Finger joint locking
• GEMSS syndrome
• GMS syndrome
• Goniodysgenesis
• Haspeslagh Fryns Muelenaere syndrome
• Hennekam Beemer syndrome
• Heritable disorder of neutrophil function
• Hip pathological dislocation
• Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome
• Ichthyosis, short stature, brachydactyly, microspherophakia syndrome
• KBG syndrome
• Larsen-like osseous dysplasia, short stature syndrome
• Lentiglobus
• Lentiglobus
• Loose anagen hair syndrome
• Macrocephaly, short stature, paraplegia syndrome
• MAGEL2-related Prader-Willi-like syndrome
• Microphakia
• Microphakia
• Microspherophakia
• Microspherophakia
• Microtia
• Mulibrey nanism syndrome
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, small stature, without skeletal dysplasia
• Neck webbing
• Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
• Noonan syndrome-like disorder with loose anagen hair
• Noonan's syndrome
• Oliver McFarlane syndrome
• Osteodysplastic primordial dwarfism
• Osteodysplastic primordial dwarfism, type 1
• Prader-Willi-like syndrome
• Prader-Willi-like syndrome
• Robin sequence
• Robinow syndrome
• Rud's syndrome
• Russell-Silver syndrome
• Seckel syndrome
• Severe lateral tibial bowing with short stature
• Short stature Brussels type
• Short stature locking fingers syndrome
• Short stature with webbed neck and congenital heart disease syndrome
• Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
• Short stature, pituitary and cerebellar defect and small sella turcica syndrome
• SHOX-related short stature
• SIM1-related Prader-Willi-like syndrome
• Sjögren-Larsson syndrome
• Skeletal dysplasia with epilepsy and short stature syndrome
• Spherophakia
• Spherophakia
• Subaortic stenosis and short stature syndrome
• Thong Douglas Ferrante syndrome
• Trichothiodystrophy
• Trigonocephaly
• Trigonocephaly, short stature, developmental delay syndrome
• Ullrich congenital muscular dystrophy
• Urban Rogers Meyer syndrome
• Warsaw breakage syndrome
• Wiedemann Steiner syndrome
• Xeroderma pigmentosum
• Xeroderma pigmentosum and Cockayne syndrome complex
• X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome
• X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome

Diagnostic Related Group(s)

The code Q87.19 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q87.19 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Aarskog syndrome
  • Cockayne syndrome
  • De Lange syndrome
  • Dubowitz syndrome
  • Noonan syndrome
  • Robinow-Silverman-Smith syndrome
  • Russell-Silver syndrome
  • Seckel syndrome

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

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