Disease #00718 (MGORS3 (Meier-Gorlin syndrome, type 3 (MGORS-3)), OMIM:613803)

Official abbreviation MGORS3
Name Meier-Gorlin syndrome, type 3 (MGORS-3)
OMIM ID 613803
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ORC6
Associated tissues -
Disease features -
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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00155005 - PubMed: Tarailo-Graovac 2015 - M no - Chinese - - - - MGORS3 - - PIGA 1 1 Philippe Campeau
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