Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
MONDO_0016215
HPDL Causal
32707086 33188300 33970200 33634263
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities.
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Spastic paraplegia 83, autosomal recessive 1 shared geneHPDL Related via 1 shared gene including HPDL. Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities spastic paraplegia 83, autosomal recessive 1 shared geneHPDL Related via 1 shared gene including HPDL. Neurodegenerative disease 1 shared geneHPDL Related via 1 shared gene including HPDL. Spastic ataxia 1 shared geneHPDL Related via 1 shared gene including HPDL. Leigh syndrome 1 shared geneHPDL Related via 1 shared gene including HPDL.