Disease #06632 (HADDTS (Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome), OMIM:617915)

Global Variome shared LOVD

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Official abbreviation	HADDTS
Name	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
OMIM ID	617915
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CTBP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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