Disease #02602 (SPGF3 (spermatogenic failure, type 3 (SPGF-3)), OMIM:606766)

Official abbreviation SPGF3
Name spermatogenic failure, type 3 (SPGF-3)
OMIM ID 606766
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene SLC26A8
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00390051 - PubMed: Gao 2021, Journal: Gao 2021 - - no China Han Chinese - - - - SPGF3 - SLC26A8 SLC26A8 2 1 Yang Gao
00390070 - PubMed: Gao 2021, Journal: Gao 2021 - M - China Han Chinese - - - - SPGF3 - SLC26A8 SLC26A8 2 1 Yang Gao
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