ODCs

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1 OMIM reference -
1 associated gene
6 signs/symptoms

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome

Hypotrichosis-deafness syndrome

GJB2

Citations in the biomedical literature:

Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		Hypotrichosis-deafness syndrome
	Synonym(s): - Bart-Pumphrey syndrome - Knuckle pads-leuconychia-sensorineural deafness-palmoplantar keratoderma syndrome		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic 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): (no data available)

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

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 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
Hypotrichosis-deafness syndrome
(no data available)