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Metachromatic leukodystrophy, late infantile form
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Atypical Gaucher disease due to saposin C deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Metachromatic leukodystrophy, late infantile form
Atypical Gaucher disease due to saposin C deficiency

ARSA
(UniProt - OMIM)
 PSAP
(UniProt - OMIM)
PSAP
(UniProt - OMIM)

COMMON
GENES 		PSAP


Citations in the biomedical literature:


Metachromatic leukodystrophy, late infantile form
ARSA PSAP
Atypical Gaucher disease due to saposin C deficiency



Metachromatic leukodystrophy, late infantile form
Atypical Gaucher disease due to saposin C deficiency

Synonym(s):
- Arylsulfatase A deficiency, late infantile form
- MLD, late infantile form
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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.