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Distal hereditary motor neuropathy type 2

3 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Acral self-healing collodion baby

1 associated gene
1 sign/symptom

Distal hereditary motor neuropathy type 2

Acral self-healing collodion baby

HSPB1	(UniProt - OMIM)		TGM1	(UniProt - OMIM)
HSPB3	(UniProt - OMIM)
HSPB8	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HSPB1	(0.55)	TGM1

Citations in the biomedical literature:

Distal hereditary motor neuropathy type 2		Acral self-healing collodion baby
	Synonym(s): - Distal spinal muscular atrophy type 2 - dHMN2 - dSMA2		Synonym(s): - Acral SHCB

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

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

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

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Acral self-healing collodion baby
	Very frequent - Ichthyosis / ichthyosiform dermatitis
Distal hereditary motor neuropathy type 2
(no data available)