Disease #05872 (SAO (ovalocytosis, South Asian type (SAO)), OMIM:166900)

Official abbreviation SAO
Name ovalocytosis, South Asian type (SAO)
OMIM ID 166900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene SLC4A1
Associated tissues -
Disease features -
Remarks -
Date created 2020-11-08 10:47:16 +01:00 (CET)
Date last edited N/A


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     
00319388 - - - - - Tunisia - - - - - SAO - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
Legend   How to query  


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