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DO Term : autosomal recessive intellectual developmental disorder 38 [DOID:0081203] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the HERC2 gene on chromosome 15q13.

synonyms:
615516,
OMIM:615516

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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