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) |
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