Disease #05564 (SPGF24 (spermatogenic failure, type 24 (SPGF-24)), OMIM:617959)
| Official abbreviation |
SPGF24 |
| Name |
spermatogenic failure, type 24 (SPGF-24) |
| OMIM ID |
617959 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
C7orf63 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2019-02-13 22:52:06 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|