Phenotype #0000155631

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00207847
Associated disease	MOPD
Diagnosis/Initial	MOPD
Diagnosis/Definite	MOPD-1
Phenotype details	microcephaly (HP:0000252); typical brain anomalies; typical face; musculoskeletal features; radiographic findings; no other organ anomalies; skin/hair featuresm
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-12-02 14:22:28 +01:00 (CET)
Date last edited	N/A

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