Phenotype #0000223438

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00295962
Associated disease	SYNS1
Phenotype details	proximal symphalangism (HP:0100264), conductive hearing loss (HP:0000405), cutaneous syndactyly of toes (HP:0010621), Short halluces (HP:0010109)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	Multiple synostoses syndrome (SYNS1)
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Zhaoyu Pan
Database submission license	No license selected
Created by	Zhaoyu Pan
Date created	2020-03-30 17:24:29 +02:00 (CEST)
Date last edited	2020-04-01 04:00:17 +02:00 (CEST)

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