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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
29 OMIM references -
16 associated genes
No signs/symptoms info
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive nonsyndromic intellectual deficit

DNM2 CC2D1A
CRADD
CRBN
GRIK2
KIAA1033
LINS
MAN1B1
MED13L
MED23
NSUN2
PRSS12
ST3GAL3
TECR
TRAPPC9
TUSC3
ZC3H14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DNM2
(0.63)
MAN1B1



Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2
Autosomal recessive nonsyndromic intellectual deficit
CC2D1A CRADD CRBN GRIK2 KIAA1033 LINS
MAN1B1 MED13L MED23 NSUN2 PRSS12 ST3GAL3
TECR TRAPPC9 TUSC3 ZC3H14



Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive nonsyndromic intellectual deficit

Synonym(s):
- CMTDIB

Synonym(s):
- NS-ARID

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.