Microcephaly, epilepsy, cerebral and/or cerebellar atrophy and short stature

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Subtype of: Microcephaly
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
microcephaly, epilepsy, cerebral and/or cerebellar atrophy and short stature
MONDO_0014043
ZNF335 Unknown
23178126 27540107 29652087 31187448 33216650 34982360 38549403 40583037
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Microcephaly, epilepsy, cerebral and/or cerebellar atrophy and short stature.
5 View disease cluster →
Microcephalic primordial dwarfism 1 shared geneZNF335 Related via 1 shared gene including ZNF335. Aminoacylase deficiency 1 shared geneZNF335 Related via 1 shared gene including ZNF335. Autosomal recessive primary microcephaly 1 shared geneZNF335 Related via 1 shared gene including ZNF335. Aneurysm 1 shared geneZNF335 Related via 1 shared gene including ZNF335. Primary microcephaly 1 shared geneZNF335 Related via 1 shared gene including ZNF335.