Disease #05336 (IMD47 (immunodeficiency, type 47 (IMD-47)), OMIM:300972)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	IMD47
Name	immunodeficiency, type 47 (IMD-47)
OMIM ID	300972
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP6AP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-10-24 17:00:35 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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