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MIM:616291 - LICHTENSTEIN-KNORR SYNDROME; LIKNS
Xenbase Genes: slc9a1
Human Disease Resource: MIM
MONDO:0014572 - Lichtenstein-Knorr syndrome |
DOID:0080065 - autosomal recessive spinocerebellar ataxia 19 |
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MONDO:0014572 - Lichtenstein-Knorr syndrome |
DOID:0080065 - autosomal recessive spinocerebellar ataxia 19 |