Disease #04287 (myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related, OMIM:613869)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	-
Name	myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related
OMIM ID	613869
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CRYAB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-06-19 22:22:25 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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