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DO Term : ectodermal dysplasia [DOID:2121] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.

synonyms:
OMIM:PS305100,
NCI:C84683,
UMLS_CUI:C0013575,
SNOMEDCT_US_2023_03_01:8654005,
MESH:D004476,
GARD:6317,
Congenital ectodermal dysplasia,
ORDO:79373,
Congenital ectodermal defect,
PS305100,
ICD9CM:757.31

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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