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's subclass of is recorded as punctate palmoplantar keratoderma^[5].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's subclass of is recorded as autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature^[6].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's OMIM ID is recorded as 615522^[7].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's KEGG ID is recorded as H01394^[8].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's Orphanet ID is recorded as 324561^[9].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's ICD-9-CM is recorded as 757.39^[10].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's genetic association is recorded as ENPP1^[11].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_324561^[12].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's UMLS CUI is recorded as C3809781^[13].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's ICD-10-CM is recorded as Q82.8^[14].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's GARD rare disease ID is recorded as 12384^[15].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's Mondo ID is recorded as MONDO_0014227^[16].
• Hypopigmentation-punctate palmoplantar keratoderma syndrome's UniProt disease ID is recorded as DI-03946^[17].