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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Isolated growth hormone deficiency type IB

ATP11A GH1
DPP9 GHRHR
DSP
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
(0.63)
GH1



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Isolated growth hormone deficiency type IB
GH1 GHRHR



Idiopathic pulmonary fibrosis
Isolated growth hormone deficiency type IB

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Congenital IGHD type IB
- Congenital isolated GH deficiency type IB
- Congenital isolated growth hormone deficiency type IB

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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

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

No signs/symptoms info available.