Disease #00072 (DTD (dysplasia, diastrophic (DTD)), OMIM:222600)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DTD
Name	dysplasia, diastrophic (DTD)
OMIM ID	222600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC26A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 14:31:02 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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