Autosomal Domit Chondrodysplasia Punctata
Disease ID: disease_node_19141
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q77.3, MIM:118650, MIM:118651, MIM:602497, ORDO:79344 |
|---|---|
| Subclassof | DOID_0050736, DOID_2581 |
| Data Source | DOID |
| Doid Label | autosomal domit chondrodysplasia punctata |
| Doid Description | A chondrodysplasia punctata that is characterized by abnormal facies and stippling of the limbs, associated with vitamin K-related teratogenicity, has_material_basis_in autosomal domit inheritance. NT MGI. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19141 |
| Doid Id | DOID_0060293 |
| Label | Autosomal Domit Chondrodysplasia Punctata |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Chondrodysplasia Punctata(ID:disease_node_2065) (Disease)