Phenotype #0000310033

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00418738
Associated disease	MKS
Diagnosis/Initial	-
Diagnosis/Definite	Meckel-Gruber syndrome
Phenotype details	central nervous system malformation: encephalocele; cystic kidney dysplasia; ductal plate malformation; postaxial polydactyly
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-10-05 08:54:56 +02:00 (CEST)
Date last edited	N/A

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