Microcephaly 26, primary, autosomal dominant

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Subtype of: Microcephaly · Primary microcephaly
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Microcephaly 26, primary, autosomal dominant
MONDO_0030928
LMNB1 Causal
32910914 33033404
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Microcephaly 26, primary, autosomal dominant.
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Demyelinating leukodystrophy 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Primary microcephaly 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Developmental disorder 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Dyslexia 1 shared geneLMNB1 Related via 1 shared gene including LMNB1.