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DO Term : orofacial cleft 13 [DOID:0080406] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730.

synonyms:
OMIM:613857,
613857

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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