Disease #03497 (SPGF9 (spermatogenic failure, type 9 (SPGF9)), OMIM:613958)
| Official abbreviation |
SPGF9 |
| Name |
spermatogenic failure, type 9 (SPGF9) |
| OMIM ID |
613958 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DPY19L2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-11-05 09:55:19 +01:00 (CET) |
Individuals
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