ZFIN Human Disease: interstitial lung disease 2

OBO ID: DOID:0050156

Term Name:	interstitial lung disease 2		Search Ontology:
Synonyms:	cryptogenic fibrosing alveolitis FIBROCYSTIC PULMONARY DYSPLASIA idiopathic pulmonary fibrosis IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
Definition:	An interstitial lung disease pulmonary fibrosis that is characterized by scarring of the lung and that has_material_basis_in heterozygous mutation in the SFTPA2 gene on chromosome 10q22. (2)
References:	EFO:0000768 GARD:8609 ICD10CM:J84.112 ICD9CM:516.31 MESH:D054990 NCI:C35716 OMIM:178500 SNOMEDCT_US_2023_03_01:28168000 UMLS_CUI:C1800706
Ontology:	Human Disease ( DOID:0050156 )

Relationships

is a type of:	autosomal dominant disease interstitial lung disease autosomal dominant disease interstitial lung disease Show first 5 Terms

OTHER interstitial lung disease 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MUC5B		{Pulmonary fibrosis, idiopathic, susceptibility to}
SFTPA2		Interstitial lung disease 2

ZEBRAFISH MODELS

Fish	Conditions	Citations
WT	xenotransplantation	Xia et al., 2014

PHENOTYPE No data available

CITATIONS (1)