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

Charcot-Marie-Tooth disease type 4D

Hypomyelination with brain stem and spinal cord involvement and leg spasticity


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NDRG1	(0.72)	DARS

Citations in the biomedical literature:

Charcot-Marie-Tooth disease type 4D		Hypomyelination with brain stem and spinal cord involvement and leg spasticity
	Synonym(s): - CMT4D - HMSN, Lom type - Hereditary motor and sensory neuropathy, Lom type		Synonym(s): - HBSL

	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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.