Disease #03736 (SPGF10 (spermatogenic failure, type 10 (SPGF-10)), OMIM:614822)

Official abbreviation SPGF10
Name spermatogenic failure, type 10 (SPGF-10)
OMIM ID 614822
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SEPT12
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.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00107761 - - - M - Taiwan East Asian; Han-Taiwanese - - - - SPGF10 infertility; sporadic? (parents not tested) SEPT12 SEPT12 1 1 Pao-Lin Kuo
00107762 - - - M - Taiwan East Asian; Han-Taiwanese - - - - SPGF10 infertility; sporadic? (parents not tested) SEPT12 SEPT12 1 1 Pao-Lin Kuo
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.