Disease #00242 (CFSMR (dysmorphism, craniofacial, skeletal anomalies, and mental retardation syndrome (CFSMR)), OMIM:614132)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CFSMR
Name	dysmorphism, craniofacial, skeletal anomalies, and mental retardation syndrome (CFSMR)
OMIM ID	614132
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMCO1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-11 20:22:53 +02:00 (CEST)
Date last edited	2015-12-07 07:11:25 +01:00 (CET)

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