Coxoauricular syndrome

Orpha code: 1508OMIM code: 122780

Definicja

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
Klasyfikacja

Malformation syndrome

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

No additional description.

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