Bardet-Biedl Syndrome 17
Disease ID: disease_node_20215
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q87.89, MIM:615994 |
|---|---|
| Subclassof | DOID_1935 |
| Data Source | DOID |
| Synonyms | BBS17 |
| Doid Label | Bardet-Biedl syndrome 17 |
| Doid Description | A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21. |
| Disease Node Id | disease_node_20215 |
| Doid Id | DOID_0110139 |
| Label | Bardet-Biedl Syndrome 17 |
- Outgoing r'ship
SUBCLASS_OFto/from Bardet-Biedl Syndrome(ID:disease_node_10716) (Disease)