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DO Term : congenital hypotrichosis with juvenile macular dystrophy [DOID:0110711] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the CDH3 gene on chromosome 16q22.1.

synonyms:
OMIM:601553,
HJMD,
GARD:3066,
601553,
hypotrichosis with cone-rod dystrophy

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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