Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/608049
http://purl.bioontology.org/ontology/OMIM/608049
|
|---|---|
| Preferred Name | AUTISM, SUSCEPTIBILITY TO, 3 |
| Synonyms |
AUTS3
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | AUTS3
|
|---|---|
| prefLabel | AUTISM, SUSCEPTIBILITY TO, 3
|
| Gene Symbol | AUTS3
|
| Scope Statement |
Genetic heterogeneity (see 209850) [MISCELLANEOUS]
Onset by 3 years of age [MISCELLANEOUS]
Occurs in 2-5 per 10,000 individuals [MISCELLANEOUS]
Associated with Fragile X syndrome (300624) [MISCELLANEOUS]
Associated with untreated phenylketonuria (261600) [MISCELLANEOUS]
Male to female ratio 4:1 [MISCELLANEOUS]
Associated with tuberous sclerosis (191100) [MISCELLANEOUS]
See more
See less
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T033
|
| Gene Locus | 13q13.2-q14.1
|
| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
|
| notation | 608049
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1842632
|
| OMIM Entry Type | 5
|
| OMIM MimType Value | perc
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |