cataract 41
Information
- Disease name
- cataract 41
- Disease ID
- DOID:0110241
- Description
- "A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16." [url:https\://www.ncbi.nlm.nih.gov/pubmed/23531866]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:83
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q12.0
- Cross Reference ID (Disease Ontology)
- MIM:116400
- Exact Synonym (Disease Ontology)
- congenital nuclear type cataract 41
- Exact Synonym (Disease Ontology)
- CTRCT41
- MedGen concept unique identifier (MedGen Concept name)
- C3805412
- MedGen unique identifier (MedGen Concept name)
- 811742