KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4

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Summary

Literature (0)

MIM:616549 - KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4

Xenbase Genes: myo18b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014689 - Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome

MONDO:0014689 - Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome

Disease Ontology (DO):

DOID:0080592 - Klippel-Feil syndrome 4

DOID:0080592 - Klippel-Feil syndrome 4