Disease #00261 (HDL2 (Huntington disease-like, type 2 (HDL2)), OMIM:606438)
| Official abbreviation |
HDL2 |
| Name |
Huntington disease-like, type 2 (HDL2) |
| OMIM ID |
606438 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
16 |
| Phenotype entries for this disease |
16 |
| Associated with 1 gene |
JPH3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-29 08:47:24 +01:00 (CET) |
| Date last edited |
2020-10-08 08:37:05 +02:00 (CEST) |
Individuals
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