Disease #01536 (IPF (fibrosis, pulmonary, idiopathic (IPF)), OMIM:178500)

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	Curator: Johan T. den Dunnen

Official abbreviation	IPF
Name	fibrosis, pulmonary, idiopathic (IPF)
OMIM ID	178500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 4 genes	MUC5B, SFTPA1, SFTPA2, SFTPC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A