Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/617721 http://purl.bioontology.org/ontology/OMIM/617721
Preferred Name	NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 9
Synonyms	HMN9 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IX DHMN9 HMND9
Type	http://www.w3.org/2002/07/owl#Class

altLabel	HMN9 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IX DHMN9 HMND9
prefLabel	NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 9
Gene Symbol	HMND9 WARS WARS1 NEDMSBA
Scope Statement	Slowly progressive [MISCELLANEOUS] Caused by mutation in the tryptophanyl-tRNA synthetase 1 gene (WARS1, 191050.0001) [MOLECULAR BASIS] Juvenile onset (range 9 to 13 years) [MISCELLANEOUS] Lower limb involvement usually precedes upper limb involvement [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU000328 http://purl.bioontology.org/ontology/OMIM/MTHU000335 http://purl.bioontology.org/ontology/OMIM/MTHU036949 http://purl.bioontology.org/ontology/OMIM/MTHU065997 http://purl.bioontology.org/ontology/OMIM/MTHU026112 http://purl.bioontology.org/ontology/OMIM/MTHU040871 http://purl.bioontology.org/ontology/OMIM/MTHU065998 See more See less
tui	T047
Gene Locus	14q32.31
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	617721
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C4540265
OMIM Entry Type	3
OMIM MimType Value	pound

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