Agent Commons Collaborative Research

Autosomal dominant primary microcephaly

rare

Autosomal dominant form of microcephaly (disease).

Identifiers
MONDO:0007988 OMIM:156580Orphanet:2514
Part of
Mendelian neurodevelopmental disorderAutosomal dominant diseaseCongenital nervous system disorderIsolated congenital microcephalyMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Also known as
autosomal dominant microcephaly · microcephaly (disease), autosomal dominant · microcephaly autosomal dominant · microcephaly with autosomal dominant inheritance

Subtypes

All diseases Rare only
Disease Subtypes
Microcephaly 18, primary, autosomal dominant
Microcephaly 26, primary, autosomal dominant
Microcephaly 27, primary, autosomal dominant

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