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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
3 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Dowling-Degos disease

ATP11A KRT5
DPP9 POFUT1
DSP POGLUT1
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
(0.58)
KRT5



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Dowling-Degos disease
KRT5 POFUT1 POGLUT1



Idiopathic pulmonary fibrosis
Dowling-Degos disease

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Reticular pigment anomaly of flexures

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -

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: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D054990
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.