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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/618672
http://purl.bioontology.org/ontology/OMIM/618672
|
|---|---|
| Preferred Name | INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES |
| Synonyms |
IDDSADF
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | IDDSADF
|
|---|---|
| prefLabel | INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES
|
| Gene Symbol |
IDDSADF
NOT3
CNOT3
|
| Scope Statement | Caused by mutation in the CCR4-NOT transcription complex, subunit 3 gene (CNOT3, 604910.0001) [MOLECULAR BASIS]
De novo mutation [MISCELLANEOUS]
Highly variable phenotype [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 19q13.4
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 618672
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C5231456
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |