Mulibrey nanism

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MULIBREY NANISM
C05245822532502576MESH:D050336MONDO:0009664
PNPLA7 Unknown — Disgenet
PPM1E Unknown — Disgenet —
TRIM37 Unknown
14757854 19347900
CTD, ClinGen, Disgenet, GenCC, HPO, Orphanet
TRPM3 Unknown — Disgenet
All4 Causal0 Unknown4
Related Diseases Diseases that share the most curated genes with Mulibrey nanism.
5 View disease cluster →
cataract 50 with or without glaucoma 1 shared geneTRPM3 Related via 1 shared gene including TRPM3. Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development 1 shared genePNPLA7 Related via 1 shared gene including PNPLA7. Birk-barel syndrome 1 shared geneTRPM3 Related via 1 shared gene including TRPM3. Cataract-glaucoma syndrome 1 shared geneTRPM3 Related via 1 shared gene including TRPM3. Stomach disease 1 shared geneTRPM3 Related via 1 shared gene including TRPM3.