Phenotype #0000222670

Global Variome shared LOVD

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

Individual ID	00289036
Associated disease	neuropathy, optic
Phenotype details	Attention deficit (HP:0007018); Cognitive impairment (HP:0100543); Strabismus (HP:0000486)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	15y (15 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-25 16:16:02 +01:00 (CET)
Date last edited	2020-08-25 21:27:59 +02:00 (CEST)

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