Disease #03859 (PAPA6 (polydactyly, postaxial, type A6 (PAPA-6)), OMIM:615226)

Official abbreviation PAPA6
Name polydactyly, postaxial, type A6 (PAPA-6)
OMIM ID 615226
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 ZNF141
Associated tissues -
Disease features autosomal recessive
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     
00102104 BD267-4 - - M yes Pakistan Pastoon - - - - PAPA6 - MAD1L1 BAG3, MAD1L1, PNPLA4 4 1 Muhammad Umair
Legend   How to query  


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