ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal dominant Charcot-Marie-Tooth disease type 2A1

Distal 17p13.3 microdeletion syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIF1B	(0.63)	YWHAE

Citations in the biomedical literature:

Autosomal dominant Charcot-Marie-Tooth disease type 2A1		Distal 17p13.3 microdeletion syndrome
	Synonym(s): - CMT2A1		Synonym(s): - Distal del(17)(p13.3 ) - Distal monosomy 17p13.3

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

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

	Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.