amelogenesis imperfecta type 1A
Information
- Disease name
- amelogenesis imperfecta type 1A
- Disease ID
- DOID:0110054
- Description
- "An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32." [url:https\://www.ncbi.nlm.nih.gov/pubmed/23632796, url:https\://www.ncbi.nlm.nih.gov/pubmed/23958762]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:2187
- Cross Reference ID (Disease Ontology)
- ICD10CM:K00.5
- Cross Reference ID (Disease Ontology)
- MIM:104530
- Exact Synonym (Disease Ontology)
- AI1A
- Exact Synonym (Disease Ontology)
- amelogenesis imperfecta hypoplastic type IA
- Exact Synonym (Disease Ontology)
- amelogenesis imperfecta type IA