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Metachromatic leukodystrophy, late infantile form
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
Metachromatic leukodystrophy, late infantile form
Parkinsonian-pyramidal syndrome

ARSA
(UniProt - OMIM)
 FBXO7
(UniProt - OMIM)
PSAP
(UniProt - OMIM)
 SNCA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PSAP
(0.49)
SNCA


Citations in the biomedical literature:


Metachromatic leukodystrophy, late infantile form
ARSA PSAP
Parkinsonian-pyramidal syndrome
FBXO7 SNCA



Metachromatic leukodystrophy, late infantile form
Parkinsonian-pyramidal syndrome

Synonym(s):
- Arylsulfatase A deficiency, late infantile form
- MLD, late infantile form
Synonym(s):
- Pallidopyramidal syndrome
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- 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:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.