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MIM:610205 - ALAGILLE SYNDROME 2; ALGS2
Xenbase Genes: notch2
Human Disease Resource: MIM
MONDO:0007318 - Alagille syndrome |
MONDO:0012439 - Alagille syndrome due to a NOTCH2 point mutation |
Disease Ontology (DO):
DOID:9245 - Alagille syndrome |
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MONDO:0007318 - Alagille syndrome |
MONDO:0012439 - Alagille syndrome due to a NOTCH2 point mutation |
DOID:9245 - Alagille syndrome |