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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