Hypopigmentation-punctate palmoplantar keratoderma syndrome
human disease
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Hypopigmentation-punctate palmoplantar keratoderma syndrome
Summary
Hypopigmentation-punctate palmoplantar keratoderma syndrome is a hereditary disorder[1].
Key Facts
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's instance of is recorded as hereditary disorder[2].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's instance of is recorded as rare disease[3].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's instance of is recorded as class of disease[4].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome is a type of punctate palmoplantar keratoderma[5].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome is a type of autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature[6].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's ICD-9-CM is recorded as 757.39[7].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's genetic association is recorded as ENPP1[8].
- Hypopigmentation-punctate palmoplantar keratoderma syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_324561[9].