ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Porokeratotic eccrine ostial and dermal duct nevus

Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome

GJB2

Citations in the biomedical literature:

Porokeratotic eccrine ostial and dermal duct nevus		Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
	Synonym(s): - Comedo nevus of the palm - Porokeratotic eccrine nevus		Synonym(s): - Bart-Pumphrey syndrome - Knuckle pads-leuconychia-sensorineural deafness-palmoplantar keratoderma syndrome

	Classification (Orphanet): - Rare genetic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
	Very frequent - Abnormal nails colour / leukonychia / melanonychia - Autosomal dominant inheritance - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Sensorineural deafness / hearing loss - Subcutaneous nodules / lipomas / tumefaction / swelling Frequent - Palmoplantar hyperkeratosis / keratoderma
Porokeratotic eccrine ostial and dermal duct nevus
(no data available)