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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

Q87.1 – Congenital malformation syndromes predominantly associated with short stature

Overview

Coding Notes

Removed
Non-billable / Non-specific, not valid for HIPAA-covered transactions

Type 1 Excludes

Ellis-van Creveld syndrome (Q77.6)
Smith-Lemli-Opitz syndrome (E78.72)

GEM Conversion to ICD-9 CM

Fs: 10000 – Prader-Willi syndrome

Child Codes

Prader-Willi syndrome
Other congenital malformation syndromes predominantly associated with short stature

Sibling Codes

Congenital malformation syndromes predominantly affecting facial appearance
Congenital malformation syndromes predominantly involving limbs
Congenital malformation syndromes involving early overgrowth
Marfan's syndrome
Other congenital malformation syndromes with other skeletal changes
Other specified congenital malformation syndromes, not elsewhere classified

Parent Sibling Codes

Congenital ichthyosis
Epidermolysis bullosa
Other congenital malformations of skin
Congenital malformations of breast
Other congenital malformations of integument
Phakomatoses, not elsewhere classified
Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
Other specified congenital malformation syndromes affecting multiple systems
Other congenital malformations, not elsewhere classified

View in Tabular

Code Title
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Q80-Q89 Other congenital malformations (Q80-Q89)
Q87 Other specified congenital malformation syndromes affecting multiple systems
Q87.1 Congenital malformation syndromes predominantly associated with short stature
Type 1 Excludes
Ellis-van Creveld syndrome (Q77.6)
Smith-Lemli-Opitz syndrome (E78.72)

Q87.11 Prader-Willi syndrome
Q87.19 Other congenital malformation syndromes predominantly associated with short stature