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Idiopathic pulmonary arterial hypertension
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Metachromatic leukodystrophy, juvenile form
2 associated genes
No signs/symptoms info
Idiopathic pulmonary arterial hypertension
Metachromatic leukodystrophy, juvenile form

BMPR2
(UniProt - OMIM)
 ARSA
(UniProt - OMIM)
CBLN2
(UniProt - OMIM)
 PSAP
(UniProt - OMIM)
KCNK3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BMPR2
(0.52)
ARSA


Citations in the biomedical literature:


Idiopathic pulmonary arterial hypertension
BMPR2 CBLN2 KCNK3
Metachromatic leukodystrophy, juvenile form
ARSA PSAP



Idiopathic pulmonary arterial hypertension
Metachromatic leukodystrophy, juvenile form

Synonym(s):
- IPAH
Synonym(s):
- Arylsulfatase A deficiency, juvenile form
- MLD, juvenile form
Classification (Orphanet):
- Rare genetic disease
- Rare respiratory disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: adult
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.