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loading...| Preferred Name |
Fraser syndrome 1 |
| Synonyms |
FRASRS1 |
| Definitions |
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21.21. |
| ID |
http://purl.obolibrary.org/obo/DOID_0111405 |
| database_cross_reference |
OMIM:219000 |
| definition |
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21.21. |
| has exact synonym |
FRASRS1 |
| has_obo_namespace |
disease_ontology |
| id |
DOID:0111405 |
| label |
Fraser syndrome 1 |
| notation |
DOID:0111405 |
| prefLabel |
Fraser syndrome 1 |
| subClassOf |
Create New Mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/219000 | Online Mendelian Inheritance in Man | LOOM |