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SERKAL syndrome

ORPHA:139466Malformation syndromeAutosomal recessiveAntenatal

Ассоциированные гены (1)

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

Фенотипы (15)

Облигатный (100%)5
HP:0000104Renal agenesis
HP:0001510Growth delay
HP:0001562Oligohydramnios
HP:0002089Pulmonary hypoplasia
HP:0012245Sex reversal
Частый (30–79%)10
HP:0000036Abnormality of the penis
HP:0000047Hypospadias
HP:0000202Orofacial cleft
HP:0000776Congenital diaphragmatic hernia
HP:0000834Abnormality of the adrenal glands
HP:0001629Ventricular septal defect
HP:0001642Pulmonic stenosis
HP:0004794Malrotation of small bowel
HP:0005343Hypoplasia of the bladder
HP:0030680Abnormal cardiovascular system morphology

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