Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/608631 http://purl.bioontology.org/ontology/OMIM/608631
Preferred Name	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2
Synonyms	ASPG2
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ASPG2
prefLabel	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2
Gene Symbol	ASPG2
Scope Statement	Genetic heterogeneity (see 608638) [MISCELLANEOUS] Onset in early childhood [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU001941 http://purl.bioontology.org/ontology/OMIM/MTHU001935 http://purl.bioontology.org/ontology/OMIM/MTHU022122 http://purl.bioontology.org/ontology/OMIM/MTHU022121 http://purl.bioontology.org/ontology/OMIM/MTHU001934 http://purl.bioontology.org/ontology/OMIM/MTHU001936 http://purl.bioontology.org/ontology/OMIM/MTHU022120 http://purl.bioontology.org/ontology/OMIM/MTHU001937 http://purl.bioontology.org/ontology/OMIM/MTHU001938 See more See less
tui	T047
Gene Locus	17p13
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	608631
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU001943 http://purl.bioontology.org/ontology/OMIM/MTHU000251
cui	C1837697
OMIM Entry Type	5
OMIM MimType Value	perc

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