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1 OMIM reference -
11 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 3
8 OMIM references -
6 associated genes
12 signs/symptoms
Idiopathic pulmonary fibrosis
Familial melanoma

ATP11A CDK4
DPP9 CDKN2A
DSP CDKN2B
FAM13A CDKN2D
MUC5B MC1R
OBFC1 TERT
SFTPA1
SFTPA2
SFTPC
TERC
TERT


COMMON
GENES
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TERC
TERC
TERC
(0.63)
(0.63)
(0.63)
CDK4
CDKN2A
TERT



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Familial melanoma
CDK4 CDKN2A CDKN2B CDKN2D MC1R



Idiopathic pulmonary fibrosis
Familial melanoma

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Neoplasms -

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:
8 OMIM references -
No MeSH references

Familial melanoma

Very frequent
- Capillary hemangioma / nevus / naevus flammeus / port-wine stain
- Melanoma

Frequent
- Anomalies of the lymphatic system
- Dry / squaly skin / exfoliation
- Excessive freckling
- Hair and scalp anomalies

Occasional
- Autosomal dominant inheritance
- Breast neoplasm / tumor / carcinoma / cancer
- Estomach / gastric neoplasm / tumor / carcinoma / cancer
- Extrapyramidal syndrome
- Pancreatic / pancreas neoplasm / tumor / carcinoma / cancer
- Retinopathy


Idiopathic pulmonary fibrosis

(no data available)