Alport syndrome with mental retardation midface hypoplasia and elliptocytosis

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Subtype of: Alport syndrome
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Alport syndrome with mental retardation midface hypoplasia and elliptocytosis
MONDO_0010263
ACSL4 Unknown
11889465 12525535
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Alport syndrome with mental retardation midface hypoplasia and elliptocytosis.
5 View disease cluster →
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome 1 shared geneACSL4 Related via 1 shared gene including ACSL4. Amme complex 1 shared geneACSL4 Related via 1 shared gene including ACSL4. Non-syndromic X-linked intellectual disability 1 shared geneACSL4 Related via 1 shared gene including ACSL4. X-linked intellectual disability 1 shared geneACSL4 Related via 1 shared gene including ACSL4. Intellectual developmental disorder, x-linked 1 shared geneACSL4 Related via 1 shared gene including ACSL4.