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1 OMIM reference -
11 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 2
3 OMIM references -
3 associated genes
4 signs/symptoms
Idiopathic pulmonary fibrosis
Keratosis palmoplantaris striata

ATP11A DSG1
DPP9 DSP
DSP KRT1
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


COMMON
GENES
DSP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
TERC
(0.78)
(0.63)
KRT1
KRT1



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Keratosis palmoplantaris striata
DSG1 KRT1



Idiopathic pulmonary fibrosis
Keratosis palmoplantaris striata

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Keratosis palmoplantaris striata et areata
- Keratosis palmoplantaris varians of Wachters
- Striate palmoplantar keratoderma

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

Keratosis palmoplantaris striata

Very frequent
- Autosomal dominant inheritance
- Palmoplantar hyperkeratosis / keratoderma

Frequent
- Hair and scalp anomalies
- Nails anomalies



Idiopathic pulmonary fibrosis

(no data available)