Microcephaly, seizures, and developmental delay

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Developmental delay and microcephaly · Microcephaly
Show the subtype
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Microcephaly, seizures, and developmental delay
MONDO_0013254
PNKP Causal
20118933 27066567 27232581 28453785 30039206
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Microcephaly, seizures, and developmental delay.
5 View disease cluster →
Dna repair-deficiency disorders 1 shared genePNKP Related via 1 shared gene including PNKP. Ataxia with oculomotor apraxia 1 shared genePNKP Related via 1 shared gene including PNKP. Pyridoxine dependent epilepsy 1 shared genePNKP Related via 1 shared gene including PNKP. Cerebellar atrophy 1 shared genePNKP Related via 1 shared gene including PNKP. Congenital microcephaly 1 shared genePNKP Related via 1 shared gene including PNKP.