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Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome

ORPHA:363523DiseaseAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

COG6
component of oligomeric golgi complex 6
Disease-causing germline mutation(s) in
OMIM: 606977

Фенотипы (16)

Частый (30–79%)12
HP:0000455Broad nasal tip
HP:0000670Carious teeth
HP:0000750Delayed speech and language development
HP:0000966Hypohidrosis
HP:0000972Palmoplantar hyperkeratosis
HP:0001249Intellectual disability
HP:0001954Recurrent fever
HP:0002205Recurrent respiratory infections
HP:0005338Sparse lateral eyebrow
HP:0006297Enamel hypoplasia
HP:0012434Delayed social development
HP:0012471Thick vermilion border
Периодический (5–29%)3
HP:0005484Secondary microcephaly
HP:0012115Hepatitis
HP:0040196Mild microcephaly
Исключён (0%)1
HP:0003160Abnormal isoelectric focusing of serum transferrin

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