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

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

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


Citations in the biomedical literature:


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



Metachromatic leukodystrophy, adult form
Idiopathic pulmonary arterial hypertension

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