Disease #03727 (SOPH (stature, short, optic nerve atrophy, and pelger-huet anomaly (SOPH)), OMIM:614800)

Official abbreviation SOPH
Name stature, short, optic nerve atrophy, and pelger-huet anomaly (SOPH)
OMIM ID 614800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NBAS
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     
00271297 ED2150 Ritelli et al., 2020 submitted - M no Italy - - - - - LFIT2, MRXSC, SOPH - CUL4B, NBAS CUL4B, NBAS 3 1 Marco Ritelli
Legend   How to query  


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