Phakomatosis pigmentokeratotica

MONDO:0017317

Phakomatosis pigmentokeratotica (PPK) is a very rare epidermal nevus disorder characterized by the association of speckled lentiginous nevi with epidermal sebaceous nevi, and extracutaneous anomalies.

Also known as: Phacomatosis pigmentokeratotica, organoid nevus with sebaceous differentiation, a speckled-lentiginous nevus, and other associated anomalies

1442 clinical trials for this condition and its sub-types, 0 tagged with Phakomatosis pigmentokeratotica itself.

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Where it sits in the disease tree

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↑ Hereditary neurological disease (5791) ↑ Developmental defect during embryogenesis (1060) ↑ Hereditary skin disorder (885) ↑ Neurocutaneous syndrome (171) ↑ Nervous system benign neoplasm (87) ↑ Melanocytic nevus (77)

Including sub-types (1442) Tagged with Phakomatosis pigmentokeratotica (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.