All diseases

OMIM ID
178500
OMIM term:
PULMONARY FIBROSIS, IDIOPATHIC; IPF
Alternative terms:
IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
FIBROSING ALVEOLITIS, CRYPTOGENIC
FIBROCYSTIC PULMONARY DYSPLASIA INTERSTITIAL PNEUMONITIS, USUAL, INCLUDED; UIP, INCLUDED
HAMMAN-RICH DISEASE, INCLUDED
(∗) Location:
10q22.3   11p15.5   3q26.2   5p15.33  
(†) Associated OMIM genes:
MUC5B   SFTPA1   SFTPA2   TERC   TERT  
(‡) Associated MGI genes:

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