Disease #01124 (mental retardation, X-linked, syndromic, Martin-Probst type, OMIM:300519)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	-
Name	mental retardation, X-linked, syndromic, Martin-Probst type
OMIM ID	300519
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAB40AL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2015-12-08 23:50:05 +01:00 (CET)

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