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MIM:616038 - NEU-LAXOVA SYNDROME 2; NLS2
Xenbase Genes: psat1
Human Disease Resource: MIM
MONDO:0000179 - haemolymphatic fluid |
MONDO:0009736 - Neu-Laxova syndrome 1 |
MONDO:0014466 - subarachnoid fissure |
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MONDO:0000179 - haemolymphatic fluid |
MONDO:0009736 - Neu-Laxova syndrome 1 |
MONDO:0014466 - subarachnoid fissure |