Phenotype #0000051925

Individual ID	00072220
Associated disease	LGMDR3;LGMD2D
Phenotype details	proximal muscle weakness (HP:0003701), loss of ambulation (HP:0002540), respiratory impairment (HP:0002093)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	<05y
Phenotype/Onset	easy falling (HP:?)
Protein	-
Owner name	Jamie Zeegers
Database submission license	No license selected
Created by	Jamie Zeegers
Date created	2016-06-01 10:27:45 +02:00 (CEST)
Date last edited	2017-02-18 21:18:16 +01:00 (CET)

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