ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
No signs/symptoms info

Charcot-Marie-Tooth disease type 4A

17q11 microdeletion syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GDAP1	(0.63)	SUZ12

Citations in the biomedical literature:

Charcot-Marie-Tooth disease type 4A		17q11 microdeletion syndrome
	Synonym(s): - CMT4A		Synonym(s): - Del(17)(q11) - Monosomy 17q11 - NF1 microdeletion syndrome - Neurofibromatosis type 1 microdeletion syndrome

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare renal disease - Rare skin disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C535419		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.