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MIM:618651 - HALPERIN-BIRK SYNDROME; HLBKS
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0032849 - neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies |
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MONDO:0032849 - neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies |