Phenotype #0000155645

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Individual ID	00207861
Associated disease	?
Diagnosis/Initial	-
Diagnosis/Definite	MOPD-1
Phenotype details	see paper; prenatal and postnatal growth retardation, microcephaly, developmental delay, cataract, hearing loss, dysmorphic features, ...
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-12-02 15:01:12 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.