Bart-Pumphrey syndrome
Human disease
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Bart-Pumphrey syndrome
Summary
Bart-Pumphrey syndrome is a head and neck disease[1].
Key Facts
- Bart-Pumphrey syndrome's instance of is recorded as head and neck disease[2].
- Bart-Pumphrey syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Bart-Pumphrey syndrome's instance of is recorded as rare disease[4].
- Bart-Pumphrey syndrome's instance of is recorded as class of disease[5].
- Bart-Pumphrey syndrome is a type of autosomal dominant disease[6].
- Bart-Pumphrey syndrome is a type of syndromic genetic deafness[7].
- Bart-Pumphrey syndrome is a type of autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature[8].
- Bart-Pumphrey syndrome is a type of syndrome[9].
- Bart-Pumphrey syndrome's symptoms and signs is recorded as Knuckle pads[10].
- Bart-Pumphrey syndrome's ICD-9-CM is recorded as 759.89[11].
- Bart-Pumphrey syndrome's health specialty is recorded as dermatology[12].
- Bart-Pumphrey syndrome's genetic association is recorded as GJB2[13].
- Bart-Pumphrey syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050658[14].
- Bart-Pumphrey syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050658[15].
- Bart-Pumphrey syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2698[16].
- Bart-Pumphrey syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].