|
| General Information | |||
|---|---|---|---|
| Term | Dubowitz syndrome | ID (Ontology) | DOID:14796 (Human Disease) |
| Definition | A syndrome that is characterized by microcephaly, growth retardation and a characteristic facial appearance including but not limited to narrow or triangular shaped head, micrognathia, ptosis, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids. | ||
| Also Known As | "Dubowitz's syndrome" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal recessive disease__ disease | |__syndrome_____________________| Dubowitz syndrome |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal recessive disease syndrome |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:6290 ICD10CM:Q87.19 MEDDRA:10059589 MESH:C535718 MIM:223370 NCI:C125591 SNOMEDCT_US_2023_03_01:2593002 UMLS_CUI:C0175691 |
|||