Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/608638 http://purl.bioontology.org/ontology/OMIM/608638
Preferred Name	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1
Synonyms	ASPG1
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ASPG1
prefLabel	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1
Gene Symbol	ASPG1
Scope Statement	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/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/MTHU029774 http://purl.bioontology.org/ontology/OMIM/MTHU001938 See more See less
tui	T047
Gene Locus	3q25-q27
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	608638
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	C1837646
OMIM Entry Type	5
OMIM MimType Value	perc

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