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MIM:118450 - ALAGILLE SYNDROME 1; ALGS1
Xenbase Genes: jag1
Human Disease Resource: MIM
MONDO:0016861 - Alagille syndrome due to 20p12 microdeletion |
MONDO:0016862 - Alagille syndrome due to a JAG1 point mutation |
DOID:9245 - Alagille syndrome |
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MONDO:0016861 - Alagille syndrome due to 20p12 microdeletion |
MONDO:0016862 - Alagille syndrome due to a JAG1 point mutation |
DOID:9245 - Alagille syndrome |