Phenotype #0000106401

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00133651
Associated disease	ID
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Isolated (sporadic)
Phenotype details	profound intellectual disability (HP:0002187); profound global developmental delay (HP:0012736); no speech (HP:0001344)
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Bernt Popp
Database submission license	No license selected
Created by	Bernt Popp
Date created	2017-11-16 12:41:23 +01:00 (CET)
Date last edited	2020-05-12 12:33:06 +02:00 (CEST)

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