Disease #00200 (SPGFY2 (spermatogenic failure, Y-linked, type 2 (SPGFY-2)), OMIM:415000)

Official abbreviation SPGFY2
Name spermatogenic failure, Y-linked, type 2 (SPGFY-2)
OMIM ID 415000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Y-linked
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene USP9Y
Associated tissues -
Disease features -
Remarks -
Date created 2013-09-14 20:59:13 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00002701 - PubMed: Sun 1999 - M - United States - - - - - SPGFY2 azoospermic, infertile USP9Y USP9Y 1 1 Johan den Dunnen
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