Search Ontology:
Human Disease
orofacial cleft 13
- Term ID
- DOID:0080406
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models