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Metachromatic leukodystrophy, juvenile form
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Synaptic congenital myasthenic syndromes
1 OMIM reference -
2 associated genes
No signs/symptoms info
Metachromatic leukodystrophy, juvenile form
Synaptic congenital myasthenic syndromes

ARSA
(UniProt - OMIM)
 COLQ
(UniProt - OMIM)
PSAP
(UniProt - OMIM)
 LAMB2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PSAP
(0.63)
LAMB2


Citations in the biomedical literature:


Metachromatic leukodystrophy, juvenile form
ARSA PSAP
Synaptic congenital myasthenic syndromes
COLQ LAMB2



Metachromatic leukodystrophy, juvenile form
Synaptic congenital myasthenic syndromes

Synonym(s):
- Arylsulfatase A deficiency, juvenile form
- MLD, juvenile form
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.