ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

FG syndrome type 1

Charcot-Marie-Tooth disease type 2B2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MED12	(0.73)	MED25

Citations in the biomedical literature:

FG syndrome type 1		Charcot-Marie-Tooth disease type 2B2
	Synonym(s): - Opitz-Kaveggia syndrome		Synonym(s): - AR-CMT2B2 - Autosomal recessive axonal CMT4C3 - Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537991

No signs/symptoms info available.