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Monoamine oxidase A deficiency
1 associated gene
1 connected disease
3 signs/symptoms
Disease Type of connection
Charcot-Marie-Tooth disease type 4D
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
MAOA P21397309850
Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Psychic / behavioural troubles
- X-linked recessive inheritance