Disease #00558 (ALGS2 (Alagille syndrome, type 2 (ALGS-2)), OMIM:610205)

Official abbreviation ALGS2
Name Alagille syndrome, type 2 (ALGS-2)
OMIM ID 610205
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NOTCH2
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00081092 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - ALGS2 Alagille syndrome 2 (OMIM:610205) NOTCH2 NOTCH2 1 1 Daniel Trujillano
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