Disease #05626 (PPD1 (polydactyly, preaxial I (PPD-1)), OMIM:174400)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PPD1
Name	polydactyly, preaxial I (PPD-1)
OMIM ID	174400
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GLI1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-07-23 08:52:14 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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