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Browse result for Laminin alpha 2-related dystrophy
※ introduction An alpha thalassemia that has_material_basis_in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others.
Reference
DiseaseOntology: Laminin alpha 2-related dystrophy
Reference
DiseaseOntology: Laminin alpha 2-related dystrophy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD04590 | P24043 | 3908 | LAMA2 | Laminin subunit alpha-2 | Homo sapiens |