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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