Disease #06536 (KFS4 (Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism), OMIM:616549)

Official abbreviation	KFS4
Name	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism
OMIM ID	616549
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYO18B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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

Global Variome shared LOVD