Larsen syndrome
Information
- Disease name
- Larsen syndrome
- Disease ID
- DOID:14764
- Description
- "A syndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities." [url:http\://en.wikipedia.org/wiki/Larsen_syndrome, url:https\://ghr.nlm.nih.gov/condition/larsen-syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:225
- Cross Reference ID (Disease Ontology)
- GARD:6860
- Cross Reference ID (Disease Ontology)
- MESH:C580241
- Cross Reference ID (Disease Ontology)
- MIM:150250
- Exact Synonym (Disease Ontology)
- dominant larsen syndrome
- MedGen concept unique identifier (MedGen Concept name)
- C0175778
- MedGen unique identifier (MedGen Concept name)
- 104500