Type II diabetes mellitus

Symptom Information:

Symptom ID: HPO:0005978
Synonyms:
Noninsulin dependent diabetes mellitus (NIDDM) [HPO:0005978]
Diabetes mellitus type 2 [HPO:0005978]
Diabetes mellitus Type II [HPO:0005978]
Diabetes mellitus, noninsulin-dependent [HPO:0005978]
NIDDM diabetes mellitus [HPO:0005978]
Noninsulin-dependent diabetes [HPO:0005978]
Noninsulin-dependent diabetes mellitus [HPO:0005978]
Type II Diabetes mellitus [Orphanet:41630]
Diabetes mellitus type 2 (disorder) [Orphanet:41630]
Diabetes Mellitus, Non-Insulin-Dependent [Orphanet:41630]
Diabetes mellitus, noninsulin-dependent [OMIM:Diabetes mellitus, noninsulin-dependent]
Noninsulin-dependent diabetes [OMIM:Noninsulin-dependent diabetes]
Noninsulin-dependent diabetes mellitus [OMIM:Noninsulin-dependent diabetes mellitus]
Insulin-independent/type 2 diabetes [Orphanet:41630]
Type 2 diabetes mellitus [Orphanet:41630]
Type 2 diabetes mellitus [MedDRA:10067585]
Diabetes mellitus maturity onset [MedDRA:10067585]
Diabetes mellitus non insulin-dep [MedDRA:10067585]
Diabetes mellitus non-insulin-dependent [MedDRA:10067585]
Maturity onset diabetes [MedDRA:10067585]
Maturity-onset diabetes of the young [MedDRA:10067585]
NIDDM [MedDRA:10067585]
Non-insulin-dependent diabetes mellitus [MedDRA:10067585]
Type II diabetes mellitus [MedDRA:10067585]
Type II diabetes mellitus without mention of complication [MedDRA:10067585]
Type II non-obese diabetic [MedDRA:10067585]
Type II obese diabetic [MedDRA:10067585]
Diabetes mellitus, type 2 (rare) [OMIM:Diabetes mellitus, type 2 (rare)]
Maturity-onset diabetes of the young (MODY) [OMIM:Maturity-onset diabetes of the young (MODY)]
Quality:
Cross references:
Orphanet:41630 "Insulin-independent/type 2 diabetes" [Orphanet:41630]
OMIM: "Diabetes mellitus, noninsulin-dependent" [OMIM:Diabetes mellitus, noninsulin-dependent]
OMIM: "Noninsulin-dependent diabetes" [OMIM:Noninsulin-dependent diabetes]
OMIM: "Noninsulin-dependent diabetes mellitus" [OMIM:Noninsulin-dependent diabetes mellitus]
OMIM: "Diabetes mellitus, type 2 (rare)" [OMIM:Diabetes mellitus, type 2 (rare)]
OMIM: "Maturity-onset diabetes of the young (MODY)" [OMIM:Maturity-onset diabetes of the young (MODY)]
UMLS:C0011860 "Diabetes Mellitus, Non-Insulin-Dependent" [Orphanet:41630]
Is a (Direct Parents):
MedDRA Diabetes mellitus
Orphanet Diabetes mellitus
HPO         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)
             Type II diabetes mellitus(HPO:0005978)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Diabetes mellitus(HPO:0000819)
                   Type II diabetes mellitus(HPO:0005978)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424)
       Diabetes mellitus(HPO:0000819)
          Type II diabetes mellitus(HPO:0005978)
Database Frequency: 68 / 7739
Resource:

All diseases associated with this symptom:

48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
AREDYLD syndrome (Orphanet:1133)
Acanthosis nigricans (Orphanet:924)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Alpha-mannosidosis (Orphanet:61)
Alström syndrome (Orphanet:64)
Ataxia-telangiectasia (Orphanet:100)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Autosomal dominant cerebellar ataxia (Orphanet:99)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bloom syndrome (Orphanet:125)
Carney complex (Orphanet:1359)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
DIABETES MELLITUS, NONINSULIN-DEPENDENT (OMIM:125853)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (OMIM:610374)
Down syndrome (Orphanet:870)
Flynn-Aird syndrome (Orphanet:2047)
Gastrocutaneous syndrome (Orphanet:2069)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Growth hormone insensitivity syndrome (Orphanet:181393)
Insulin-resistance syndrome type A (Orphanet:2297)
Kennedy disease (Orphanet:481)
LIG4 syndrome (Orphanet:99812)
Laurence-Moon syndrome (Orphanet:2377)
Leprechaunism (Orphanet:508)
Leukonychia totalis (Orphanet:2387)
MELAS (Orphanet:550)
MODY syndrome (Orphanet:552)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Maternally-inherited diabetes and deafness (Orphanet:225)
Maturity-onset diabetes of the young, type 1 (OMIM:125850)
Maturity-onset diabetes of the young, type 10 (OMIM:613370)
Maturity-onset diabetes of the young, type 11 (OMIM:613375)
Maturity-onset diabetes of the young, type 13 (OMIM:616329)
Maturity-onset diabetes of the young, type 14 (OMIM:616511)
Maturity-onset diabetes of the young, type 2 (OMIM:125851)
Maturity-onset diabetes of the young, type 3 (OMIM:600496)
Maturity-onset diabetes of the young, type 4 (OMIM:606392)
Maturity-onset diabetes of the young, type 6 (OMIM:606394)
Maturity-onset diabetes of the young, type 7 (OMIM:610508)
Maturity-onset diabetes of the young, type 8, with exocrine dysfunction (OMIM:609812)
Maturity-onset diabetes of the young, type 9 (OMIM:612225)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus (Orphanet:2579)
Myopathy and diabetes mellitus (Orphanet:2596)
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys (Orphanet:79118)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
POEMS syndrome (Orphanet:2905)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Prader-Willi syndrome (Orphanet:739)
Primary lipodystrophy (Orphanet:90970)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal cysts and diabetes syndrome (Orphanet:93111)
Retinitis pigmentosa (Orphanet:791)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Skeletal dysplasia - intellectual deficit (Orphanet:1436)
Stiff skin syndrome (Orphanet:2833)
Stimmler syndrome (Orphanet:3199)
Subaortic stenosis - short stature (Orphanet:3191)
Williams syndrome (Orphanet:904)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked sideroblastic anemia (Orphanet:75563)