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

Pilomatrixoma

Autosomal recessive axonal neuropathy with neuromyotonia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.82)	HINT1

Citations in the biomedical literature:

Pilomatrixoma		Autosomal recessive axonal neuropathy with neuromyotonia
	Synonym(s): - Epithelioma calcificans of Malherbe - Pilomatricoma		Synonym(s): - ARAN-NM - ARCMT2-NM - Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

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

	External references: 1 OMIM reference - 1 MeSH reference: D018296		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.