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Müllerian aplasia and hyperandrogenism

ORPHA:247768Malformation syndromeAutosomal dominant, Not applicableInfancy, Neonatal

Ассоциированные гены (1)

WNT4
Wnt family member 4
Disease-causing germline mutation(s) (loss of function) in
OMIM: 603490

Фенотипы (22)

Очень частый (80–99%)10
HP:0000013Hypoplasia of the uterus
HP:0000142Abnormality of the vagina
HP:0000786Primary amenorrhea
HP:0001007Hirsutism
HP:0001061Acne
HP:0002292Frontal balding
HP:0004322Short stature
HP:0009890High anterior hairline
HP:0009937Facial hirsutism
HP:0030088Increased serum testosterone level
Частый (30–79%)1
HP:0001513Obesity
Периодический (5–29%)11
HP:0000104Renal agenesis
HP:0000137Abnormality of the ovary
HP:0000175Cleft palate
HP:0000322Short philtrum
HP:0000411Protruding ear
HP:0000470Short neck
HP:0000574Thick eyebrow
HP:0000664Synophrys
HP:0000914Shield chest
HP:0001156Brachydactyly
HP:0002967Cubitus valgus

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы