Disease #00726 (SCN4 (neutropenia, severe congenital, type 4, autosomal recessive (SCN-4)), OMIM:612541)

Official abbreviation SCN4
Name neutropenia, severe congenital, type 4, autosomal recessive (SCN-4)
OMIM ID 612541
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene G6PC3
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

1 entry on 1 page. Showing entry 1.
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     
00266347 265977 - - F - Canada Canadian - - - - SCN4 - SCN4A SCN4A 1 1 Clinique des maladies neuromusculaires
Legend   How to query  


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