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ADULT syndrome

ORPHA:978Malformation syndromeAutosomal dominantAntenatal, Neonatal

Ассоциированные гены (1)

TP63
tumor protein p63
Disease-causing germline mutation(s) in
OMIM: 603273

Фенотипы (24)

Очень частый (80–99%)15
HP:0000164Abnormality of the dentition
HP:0000579Nasolacrimal duct obstruction
HP:0000958Dry skin
HP:0000963Thin skin
HP:0000995Melanocytic nevus
HP:0001480Freckling
HP:0001597Abnormality of the nail
HP:0001770Toe syndactyly
HP:0001803Nail pits
HP:0001839Split foot
HP:0002213Fine hair
HP:0006101Finger syndactyly
HP:0100797Toenail dysplasia
HP:0100798Fingernail dysplasia
HP:0200042Skin ulcer
Частый (30–79%)6
HP:0001596Alopecia
HP:0002209Sparse scalp hair
HP:0002557Hypoplastic nipples
HP:0002561Absent nipple
HP:0003187Breast hypoplasia
HP:0006482Abnormal dental morphology
Периодический (5–29%)3
HP:0000271Abnormality of the face
HP:0000426Prominent nasal bridge
HP:0000431Wide nasal bridge

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы