Disease #06958 (SPGFX4 (spermatogenic failure, X-linked, type 4), OMIM:301077)
| Official abbreviation |
SPGFX4 |
| Name |
spermatogenic failure, X-linked, type 4 |
| OMIM ID |
301077 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACRC |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-08-19 17:17:03 +02:00 (CEST) |
| Date last edited |
N/A |
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