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Agnathie-Holoprosenzephalie-Situs inversus-Syndrom

ORPHA:990· ICD-10 Q87.8· Agnathia-holoprosencephaly-situs inversus syndrome

Prävalenz
<1 / 1 000 000
Vererbung
Autosomal dominant, Autosomal recessive, Not applicable
Erkrankungsalter
Antenatal, Neonatal