Disease #00004 (CF (CYSTIC FIBROSIS), OMIM:219700)

Official abbreviation CF
Name CYSTIC FIBROSIS
OMIM ID 219700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CFTR
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.