loading...| Preferred Name | Paraganglioma and gastric stromal sarcoma | |
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| Definitions |
(PGGSS): Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_606864 |
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| definition |
(PGGSS): Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance. |
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| has_obo_namespace |
cell_cycle_ontology |
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| id |
OMIM:606864 |
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| label |
Paraganglioma and gastric stromal sarcoma |
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| notation |
OMIM:606864 |
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| prefLabel |
Paraganglioma and gastric stromal sarcoma |
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| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/606864 | OMIM | LOOM | |
| http://identifiers.org/omim/606864 | REXO | LOOM | |
| http://identifiers.org/omim/606864 | GEXO | LOOM | |
| http://identifiers.org/omim/606864 | RETO | LOOM |