Disease #02696 (HLD7 (leukodystrophy, hypomyelinating, type 7 (HLD7)), OMIM:607694)

Official abbreviation HLD7
Name leukodystrophy, hypomyelinating, type 7 (HLD7)
OMIM ID 607694
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene POLR3A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-01-15 19:28:31 +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     
00107928 - PubMed: Saitsu 2011 - M - - - - - - - HLD7 Diffuse cerebral hypomyelination with cerebellar atrophy, hypoplasia of corpus callosum; HCAHC POLR3A POLR3A 2 1 Johan den Dunnen
00319994 - - - - no Japan - - - - - HLD7 - - POLR3A 2 1 Hiroshi Doi
Legend   How to query  


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