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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
CLN10 disease
Metachromatic leukodystrophy, late infantile form

CTSD ARSA
PSAP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTSD
(0.84)
PSAP



Citations in the biomedical literature:


CLN10 disease
CTSD
Metachromatic leukodystrophy, late infantile form
ARSA PSAP



CLN10 disease
Metachromatic leukodystrophy, late infantile form

Synonym(s):
- Cathepsin D deficiency

Synonym(s):
- Arylsulfatase A deficiency, late infantile form
- MLD, late infantile form

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.