Disease #01539 (RTADD (acidosis, tubular, renal, distal, autosomal dominant (RTADD)), OMIM:179800)

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Official abbreviation	RTADD
Name	acidosis, tubular, renal, distal, autosomal dominant (RTADD)
OMIM ID	179800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC4A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A