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| Term | familial hyperinsulinemic hypoglycemia 7 | ID (Ontology) | DOID:0070214 (Human Disease) |
| Definition | A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has_material_basis_in mutation in the SLC16A1 gene on chromosome 1p13.2. | ||
| Also Known As | "EIHI" ; "exercise-induced hyperinsulinemic hypoglycemia" ; "exercise-induced hyperinsulinism" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease_____ hypoglycemia | |__hyperinsulinemic hypoglycemia__| familial hyperinsulinemic hypoglycemia 7 2 rec. |
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| Is a |
autosomal dominant disease hyperinsulinemic hypoglycemia |
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External Crossreferences & Linkouts
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GARD:9932 MESH:C538376 MIM:610021 NCI:C131839 ORDO:165991 SNOMEDCT_US_2023_03_01:715830008 UMLS_CUI:C1864902 |
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