Phenotype #0000209231

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00274289
Associated disease	OPPG
Phenotype details	microphthalmia (HP:0000568), fractures (HP:0002757)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	osteoporosis-pseudoglioma syndrome
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jasmine Chen
Database submission license	No license selected
Created by	Jasmine Chen
Date created	2019-12-27 23:01:33 +01:00 (CET)
Date last edited	2020-01-10 09:43:05 +01:00 (CET)

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