Disease #05732 (SRTD18 (dysplasia, short-rib thoracic, type 18 with polydactyly (SRTD18)), OMIM:617866)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SRTD18
Name	dysplasia, short-rib thoracic, type 18 with polydactyly (SRTD18)
OMIM ID	617866
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT43
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-25 16:11:22 +02:00 (CEST)
Date last edited	2020-04-25 16:12:08 +02:00 (CEST)

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