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Human Disease

orofacial cleft 13

Term ID
DOID:0080406
Synonyms
Definition
An orofacial cleft characterized by autosomal doninant inhertitance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730. https://www.ncbi.nlm.nih.gov/pubmed/21295280
References
Ontology
Human Disease   ( DOID:0080406 )
Relationships
is a type of
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Genes Involved
Zebrafish Models