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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
3 OMIM references -
5 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Autoimmune lymphoproliferative syndrome

ATP11A CASP10
DPP9 FAS
DSP FASLG
FAM13A NRAS
MUC5B PRKCD
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
TERC
(0.52)
(0.49)
CASP10
FASLG



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Idiopathic pulmonary fibrosis
Autoimmune lymphoproliferative syndrome

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D054990
External references:
3 OMIM references -
1 MeSH reference: D056735

No signs/symptoms info available.