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Metachromatic leukodystrophy, adult form
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Male infertility with normal virilization due to meiosis defect
4 OMIM references -
3 associated genes
No signs/symptoms info
Metachromatic leukodystrophy, adult form
Male infertility with normal virilization due to meiosis defect

ARSA
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
PSAP
(UniProt - OMIM)
 SOHLH1
(UniProt - OMIM)
SYCP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PSAP
(0.72)
CFTR


Citations in the biomedical literature:


Metachromatic leukodystrophy, adult form
ARSA PSAP
Male infertility with normal virilization due to meiosis defect
CFTR SOHLH1 SYCP3



Metachromatic leukodystrophy, adult form
Male infertility with normal virilization due to meiosis defect

Synonym(s):
- Arylsulfatase A deficiency, adult form
- MLD, adult form
Synonym(s):
- Azoospermia due to maturation arrest
- Azoospermia due to meiosis defect
- Male infertility with normal virilization due to maturation arrest
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic 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: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.