OBO ID: DOID:0110052 |
Term Name: | amelogenesis imperfecta type 1B | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13. https://www.ncbi.nlm.nih.gov/pubmed/11487571 | ||
References: |
|
||
Ontology: | Human Disease ( DOID:0110052 ) |
OTHER amelogenesis imperfecta type 1B PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
ENAM | Amelogenesis imperfecta, type IB |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.