Intellectual development disorder, truncal obesity, retinal dystrophy, and micropenis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
intellectual development disorder, truncal obesity, retinal dystrophy, and micropenis
MONDO_0012423
INPP5E Unknown
19668215 19668216 23022135 23386033 24896178 25529582 26748598 30055837 31173343 34211432
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Intellectual development disorder, truncal obesity, retinal dystrophy, and micropenis.
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Joubert syndrome 1 1 shared geneINPP5E Related via 1 shared gene including INPP5E. Mental retardation, truncal obesity, retinal dystrophy, and micropenis 1 shared geneINPP5E Related via 1 shared gene including INPP5E. Congenital hypoplasia of femur 1 shared geneINPP5E Related via 1 shared gene including INPP5E. Coach syndrome 1 shared geneINPP5E Related via 1 shared gene including INPP5E. Congenital hemivertebra 1 shared geneINPP5E Related via 1 shared gene including INPP5E.