Insulin-resistant diabetes mellitus

Symptom Information:

Symptom ID: HPO:0000831
Synonyms:
Insulin resistant diabetes [HPO:0000831]
Insulin resistant diabetes mellitus [HPO:0000831]
Insulin-resistant diabetes [HPO:0000831]
Insulin resistance [Orphanet:41660]
Drug resistance to insulin (disorder) [Orphanet:41660]
Insulin Resistance [Orphanet:41660]
Insulin resistant diabetes [OMIM:Insulin resistant diabetes]
Insulin resistant diabetes mellitus [OMIM:Insulin resistant diabetes mellitus]
Insulin-resistant diabetes [OMIM:Insulin-resistant diabetes]
Insulin-resistant diabetes mellitus [OMIM:Insulin-resistant diabetes mellitus]
Insulin resistance syndrome [Orphanet:41660]
Insulin resistance syndrome [MedDRA:10022490]
Insulin resistance [MedDRA:10022489]
Diabetes mellitus, insulin-resistant [OMIM:Diabetes mellitus, insulin-resistant]
Insulin resistance (in some patients) [OMIM:Insulin resistance (in some patients)]
Insulin-resistant diabetes mellitus (onset around puberty) [OMIM:Insulin-resistant diabetes mellitus (onset around puberty)]
Insulin resistant diabetes [MedDRA:10022491]
Quality:
Cross references:
HPO:0000855 "Insulin resistance" [Orphanet:41660]
Orphanet:41660 "Insulin resistance" [Orphanet:41660]
OMIM: "Insulin resistant diabetes" [OMIM:Insulin resistant diabetes]
OMIM: "Insulin resistant diabetes mellitus" [OMIM:Insulin resistant diabetes mellitus]
OMIM: "Insulin-resistant diabetes" [OMIM:Insulin-resistant diabetes]
OMIM: "Insulin-resistant diabetes mellitus" [OMIM:Insulin-resistant diabetes mellitus]
OMIM: "Diabetes mellitus, insulin-resistant" [OMIM:Diabetes mellitus, insulin-resistant]
OMIM: "Insulin resistance (in some patients)" [OMIM:Insulin resistance (in some patients)]
OMIM: "Insulin-resistant diabetes mellitus (onset around puberty)" [OMIM:Insulin-resistant diabetes mellitus (onset around puberty)]
UMLS:C0021655 "Insulin Resistance" [Orphanet:41660]
Is a (Direct Parents):
HPO         Diabetes mellitus
HPO         Insulin resistance
Orphanet Diabetes mellitus
MedDRA Hyperglycaemic conditions NEC
MedDRA Diabetes mellitus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Diabetes mellitus(HPO:0000819)
             Insulin-resistant diabetes mellitus(HPO:0000831)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Diabetes mellitus(HPO:0000819)
                   Insulin-resistant diabetes mellitus(HPO:0000831)
                Insulin resistance(HPO:0000855)
                   Insulin-resistant diabetes mellitus(HPO:0000831)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424)
       Diabetes mellitus(HPO:0000819)
          Insulin-resistant diabetes mellitus(HPO:0000831)
       Hyperglycaemic conditions NEC(MedDRA:10020638)
          Insulin-resistant diabetes mellitus(HPO:0000831)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Bangstad syndrome (Orphanet:1227)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CORTISONE REDUCTASE DEFICIENCY 2 (OMIM:614662)
Diabetes mellitus, ketosis-prone (OMIM:612227)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
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)
Insulin-resistance syndrome type A (Orphanet:2297)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Mulibrey nanism (Orphanet:2576)
Partial acquired lipodystrophy (Orphanet:79087)
Rabson-Mendenhall syndrome (Orphanet:769)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
SHORT syndrome (Orphanet:3163)