Phenotype #0000237119

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00311871
Associated disease	RRS
Phenotype details	see paper; ..., infancy slow linear growth, acromesomelia, hypertelorism, prominent forehead
Diagnosis/Initial	Robinow syndrome
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	DRS1
Age/Examination	17y (17 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-09-29 16:10:21 +02:00 (CEST)
Date last edited	2020-09-29 19:53:38 +02:00 (CEST)

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