Orofacial Cleft 13
Disease ID: disease_node_14028
Connections displayed (default: 10).
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| Dbxref | MIM:613857 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050567 |
| Data Source | DOID |
| Doid Label | orofacial cleft 13 |
| Doid Description | An orofacial cleft characterized by autosomal domit inheritance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_14028 |
| Doid Id | DOID_0080406 |
| Label | Orofacial Cleft 13 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Orofacial Cleft(ID:disease_node_14023) (Disease)