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

Official abbreviation ALGS-2
Name syndrome, Alagille, type 2 (ALGS-2)
OMIM ID 610205
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NOTCH2
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00081092 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - 0 - - ALGS-2 Alagille syndrome 2 (OMIM:610205) NOTCH2 NOTCH2 1 1 Daniel Trujillano
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