Disease #05980 (CILD37 (dyskinesia, ciliary, primary, type 37 (CILD37)), OMIM:617577)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	CILD37
Name	dyskinesia, ciliary, primary, type 37 (CILD37)
OMIM ID	617577
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-22 15:38:23 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.