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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Idiopathic pulmonary fibrosis
Epidermolysis bullosa simplex with circinate migratory erythema

ATP11A KRT5
DPP9
DSP
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
Epidermolysis bullosa simplex with circinate migratory erythema
KRT5



Idiopathic pulmonary fibrosis
Epidermolysis bullosa simplex with circinate migratory erythema

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- EBS-migr

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

Epidermolysis bullosa simplex with circinate migratory erythema

Very frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Cutaneous rash
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment



Idiopathic pulmonary fibrosis

(no data available)