Disease #00013 (CFTR (Cystic fibrosis), OMIM:602421)

Official abbreviation CFTR
Name Cystic fibrosis
OMIM ID 602421
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene CFTR
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

Reference     

Gender     

Geographic origin     

Ethnic origin     

Population     

Remarks     

Microattribution     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00000014 Zilfalil B A et al. (2006) - - - - - - CFTR - CFTR CFTR 1 1 MyHVP
Legend   How to query