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Autosomal dominant deafness-onychodystrophy syndrome

ORPHA:79499Malformation syndromeAutosomal dominantAntenatal, Neonatal

Ассоциированные гены (1)

ATP6V1B2
ATPase H+ transporting V1 subunit B2
Disease-causing germline mutation(s) in
OMIM: 606939

Фенотипы (20)

Очень частый (80–99%)2
HP:0001817Absent fingernail
HP:0008625Severe sensorineural hearing impairment
Частый (30–79%)5
HP:0000164Abnormality of the dentition
HP:0000677Oligodontia
HP:0001199Triphalangeal thumb
HP:0001802Absent toenail
HP:0008386Aplasia/Hypoplasia of the nails
Периодический (5–29%)13
HP:0000268Dolichocephaly
HP:0000348High forehead
HP:0001057Aplasia cutis congenita
HP:0001249Intellectual disability
HP:0001250Seizure
HP:0001763Pes planus
HP:0001800Hypoplastic toenails
HP:0001999Abnormal facial shape
HP:0002465Poor speech
HP:0009778Short thumb
HP:0012554Absent thumbnail
HP:0200104Absent fifth fingernail
HP:0200141Small, conical teeth

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