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

MVZ für Humangenetik Regensburg

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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	-
Date created	2016-06-28 10:03:06 +00:00 (UTC)
Date last edited	2023-06-16 10:23:30 +00:00 (UTC)