Disease #01070 (SMAX3 (atrophy, muscular, spinal, distal, X-linked, type 3 (SMAX3)), OMIM:300489)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SMAX3
Name	atrophy, muscular, spinal, distal, X-linked, type 3 (SMAX3)
OMIM ID	300489
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP7A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-09-30 16:42:57 +02:00 (CEST)

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