Coxoauricular syndrome

Orpha code: 1508OMIM code: 122780

Definition

A rare primary bone defect, described only in a mother and her three daughters to date, characterized by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981.

Disease data
Classification

Malformation syndrome

ORPHA code
1508
OMIM code
122780
ICD10 code
Q87.1
ICD11 code
LD24.E

No additional description.

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