Disease #00997 (MGORS4 (Meier-Gorlin syndrome, type 4 (MGORS4)), OMIM:613804)

Official abbreviation MGORS4
Name Meier-Gorlin syndrome, type 4 (MGORS4)
OMIM ID 613804
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CDT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-12-01 08:48:59 +01:00 (CET)


Individuals

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00320434 - - - F no United Kingdom (Great Britain) - - - - - MGORS4 - - CDT1 2 1 Louise Bicknell
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