Meckel syndrome 2

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Subtype of: Meckel-gruber syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Meckel syndrome 2
MONDO_0011296
TMEM216 Unknown
20036350 20512146 22282472 30055837 32687549
Open Targets
Meckel syndrome, type 2
MONDO_0011296
TMEM216 Causal
20036350 20512146
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Meckel syndrome 2.
5 View disease cluster →
Joubert syndrome with oculorenal defect 1 shared geneTMEM216 Related via 1 shared gene including TMEM216. Arima syndrome 1 shared geneTMEM216 Related via 1 shared gene including TMEM216. Congenital brain malformation 1 shared geneTMEM216 Related via 1 shared gene including TMEM216. Congenital hypoplasia of part of brain 1 shared geneTMEM216 Related via 1 shared gene including TMEM216. Microgyria 1 shared geneTMEM216 Related via 1 shared gene including TMEM216.