Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
3 signs/symptoms
Charcot-Marie-Tooth disease type 4D
Monoamine oxidase A deficiency

NDRG1 MAOA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NDRG1
(0.73)
MAOA



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4D
NDRG1
Monoamine oxidase A deficiency
MAOA



Charcot-Marie-Tooth disease type 4D
Monoamine oxidase A deficiency

Synonym(s):
- CMT4D
- HMSN, Lom type
- Hereditary motor and sensory neuropathy, Lom type

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive

External references:
1 OMIM reference -
1 MeSH reference: C535716
External references:
No OMIM references
No MeSH references

Monoamine oxidase A deficiency

Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Psychic / behavioural troubles
- X-linked recessive inheritance



Charcot-Marie-Tooth disease type 4D

(no data available)