Disease #01027 (DCHE (deafness, congenital heart defects, posterior embryotoxon (DCHE)), OMIM:617992)

Official abbreviation DCHE
Name deafness, congenital heart defects, posterior embryotoxon (DCHE)
OMIM ID 617992
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene JAG1
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Individuals

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00239595 - PubMed: Le Caignec 2002 - - - - - - 0 - - DCHE see paper; … JAG1 JAG1 1 1 Johan den Dunnen
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