Microcephalic primordial dwarfism

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
microcephalic primordial dwarfism due to RTTN deficiency
RTTN Causal — ClinGen —
microcephalic primordial dwarfism due to ZNF335 deficiency
MONDO_0014043
ZNF335 Causal
29652087 34982360 27540107 33216650 40583037 31187448 38549403 23178126
Open Targets —
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Microcephalic primordial dwarfism.
5 View disease cluster →
Microcephaly, epilepsy, cerebral and/or cerebellar atrophy and short stature 1 shared geneZNF335 Related via 1 shared gene including ZNF335. Microcephaly, short stature, and polymicrogyria with seizures 1 shared geneRTTN Related via 1 shared gene including RTTN. Bilateral generalized polymicrogyria 1 shared geneRTTN Related via 1 shared gene including RTTN. Microcephaly with or without short stature 1 shared geneRTTN Related via 1 shared gene including RTTN. Aminoacylase deficiency 1 shared geneZNF335 Related via 1 shared gene including ZNF335.