Disease #00200 (SPGFY2 (spermatogenic failure, Y-linked, type 2 (SPGFY-2)), OMIM:415000)
| Official abbreviation |
SPGFY2 |
| Name |
spermatogenic failure, Y-linked, type 2 (SPGFY-2) |
| OMIM ID |
415000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Y-linked |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
USP9Y |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-09-14 20:59:13 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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