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Metachromatic leukodystrophy, late infantile form
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pulmonary venoocclusive disease
2 OMIM references -
2 associated genes
No signs/symptoms info
Metachromatic leukodystrophy, late infantile form
Pulmonary venoocclusive disease

ARSA
(UniProt - OMIM)
 BMPR2
(UniProt - OMIM)
PSAP
(UniProt - OMIM)
 EIF2AK4
(UniProt - OMIM)

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


Citations in the biomedical literature:


Metachromatic leukodystrophy, late infantile form
ARSA PSAP
Pulmonary venoocclusive disease
BMPR2 EIF2AK4



Metachromatic leukodystrophy, late infantile form
Pulmonary venoocclusive disease

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):
- Rare genetic disease
- Rare respiratory disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: D011668
No signs/symptoms info available.