Insulin resistance

Symptom Information:

Symptom ID: HPO:0000855
Synonyms:
Drug resistance to insulin (disorder) [Orphanet:41660]
Insulin Resistance [Orphanet:41660]
Insulin resistance [OMIM:Insulin resistance]
Insulin resistance [Orphanet:41660]
Insulin resistance syndrome [Orphanet:41660]
Insulin resistance syndrome [MedDRA:10022490]
Insulin resistance [MedDRA:10022489]
Insulin resistance (in some patients) [OMIM:Insulin resistance (in some patients)]
Quality:
Cross references:
HPO:0000831 "Insulin-resistant diabetes mellitus" [Orphanet:41660]
Orphanet:41660 "Insulin resistance" [Orphanet:41660]
OMIM: "Insulin resistance" [OMIM:Insulin resistance]
OMIM: "Insulin resistance (in some patients)" [OMIM:Insulin resistance (in some patients)]
UMLS:C0021655 "Insulin Resistance" [Orphanet:41660]
Is a (Direct Parents):
MedDRA Hyperglycaemic conditions NEC
Orphanet Diabetes mellitus
HPO         Abnormal glucose homeostasis
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)
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)