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Autosomal Dominant Deafness - Onychodystrophy Syndrome (MONDO:0007420)

Dominant deafness-onychodystrophy (DDOD) syndrome is a multiple congenital anomalies syndrome characterized by congenital hearing impairment, small or absent nails on the hands and feet, and small terminal phalanges.

Overview

Category

integumentary system disorder

syndromic disease

Ontology ID

MONDO:0007420

Internal:8810

Synonyms

DDOD syndrome

autosomal dominant deafness-onychodystrophy syndrome

deafness-onychodystrophy syndrome, autosomal dominant

DDOD

Ddod syndrome

Robinson Miller Bensimon syndrome

Robinson-Miller-Bensimon syndrome

deafness and onychodystrophy, dominant form

deafness, congenital, and onychodystrophy, autosomal dominant

deafness, congenital, with onychodystrophy, autosomal dominant

familial ectodermal dysplasia with sensori-neural deafness and other anomalies

Mapped terms

DOID:0080720

GARD:0004732

MEDGEN:382676

OMIM:124480

Orphanet:79499

UMLS:C2675730

Child terms

Unknown children.

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