Disease #07070 (ATS3B (Alport syndrome, type 3B, autosomal recessive), OMIM:620536)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ATS3B
Name	Alport syndrome, type 3B, autosomal recessive
OMIM ID	620536
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL4A3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-02-15 12:43:19 +01:00 (CET)
Date last edited	N/A

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