Insulin resistance
Symptom Information:
Symptom ID: | HPO:0000855 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013) Abnormal glucose homeostasis(HPO:0011014) Insulin resistance(HPO:0000855) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424) Hyperglycaemic conditions NEC(MedDRA:10020638) Insulin resistance(HPO:0000855) |
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Database Frequency: | 32 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement | (Orphanet:90301) |
Alström syndrome | (Orphanet:64) |
Bangstad syndrome | (Orphanet:1227) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CORTISONE REDUCTASE DEFICIENCY 2 | (OMIM:614662) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
DIABETES MELLITUS, NONINSULIN-DEPENDENT | (OMIM:125853) |
Diabetes mellitus, ketosis-prone | (OMIM:612227) |
Dopamine beta-hydroxylase deficiency | (Orphanet:230) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Familial symmetric lipomatosis | (Orphanet:2398) |
Friedreich ataxia 1 | (OMIM:229300) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 | (OMIM:612526) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 | (OMIM:615980) |
Leprechaunism | (Orphanet:508) |
MORBID OBESITY AND SPERMATOGENIC FAILURE | (OMIM:615703) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Primary lipodystrophy | (Orphanet:90970) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SHORT syndrome | (Orphanet:3163) |
Whipple disease | (Orphanet:3452) |