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Results: 3

Name/Gene IDDescriptionLocationAliasesMIM
ID: 100499260
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis [Homo sapiens (human)]CXDELq22.3DELXq22.3300194
ID: 9949
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Homo sapiens (human)]Chromosome X, NC_000023.11 (110194186..110440233, complement)AMMERC1300195
ID: 2182
acyl-CoA synthetase long-chain family member 4 [Homo sapiens (human)]Chromosome X, NC_000023.11 (109641335..109733392, complement)ACS4, FACL4, LACS4, MRX63, MRX68300157

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