Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/618103 http://purl.bioontology.org/ontology/OMIM/618103
Preferred Name	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 64
Synonyms	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64 MRT64
Type	http://www.w3.org/2002/07/owl#Class

altLabel	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64 MRT64
prefLabel	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 64
Gene Symbol	LRRN6A MRT64 LINGO1 LERN1
Scope Statement	Caused by mutation in the leucine-rich repeat- and Ig domain-containing NOGO receptor-interacting protein 1 gene (LINGO1, 609791.0001) [MOLECULAR BASIS] Two unrelated consanguineous Pakistani families have been reported (last curated August 2018) [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU000248 http://purl.bioontology.org/ontology/OMIM/MTHU000300 http://purl.bioontology.org/ontology/OMIM/MTHU000691 http://purl.bioontology.org/ontology/OMIM/MTHU036340 http://purl.bioontology.org/ontology/OMIM/MTHU002106 http://purl.bioontology.org/ontology/OMIM/MTHU033932 http://purl.bioontology.org/ontology/OMIM/MTHU036443 http://purl.bioontology.org/ontology/OMIM/MTHU002543 http://purl.bioontology.org/ontology/OMIM/MTHU046927 http://purl.bioontology.org/ontology/OMIM/MTHU000242 See more See less
tui	T048
Gene Locus	15q24
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	618103
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T048
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C4748192
OMIM Entry Type	3
OMIM MimType Value	pound

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