Disease #02211 (AI1E (amelogenesis imperfecta, type IE (AI1E)), OMIM:301200)
Official abbreviation |
AI1E |
Name |
amelogenesis imperfecta, type IE (AI1E) |
OMIM ID |
301200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
AMELX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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