Disease #03813 (IDDAM;AUTS18 (intellectual developmental disorder with autism and macrocephaly), OMIM:615032)
| Official abbreviation |
IDDAM;AUTS18 |
| Name |
intellectual developmental disorder with autism and macrocephaly |
| OMIM ID |
615032 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
CHD8 |
| Associated tissues |
- |
| Disease features |
0.88 behavioural problems (HP:0000708), 0.76 autism spectrum disorder or autistic behaviour (HP:0000729), 0.32 short attention span (HP:0000736), 0.31 abnormal social behaviour (HP:0012433), 0.29 sleep disturbance (HP:0002360), 0.27 impaired social interactions (HP:0000735), 0.21 stereotypy (HP:0000733), 0.20 insomnia (HP:0100785), 0.17 abnormal aggressive, impulsive or violent behaviour (HP:0006919), 0.17 impairment in personality functioning (HP:0031466), 0.16 poor eye contact (HP:0000817), 0.14 repetitive compulsive behaviour (HP:0008762) |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-08-16 16:33:07 +02:00 (CEST) |
Individuals
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