Type II diabetes mellitus
Symptom Information:
Symptom ID: | HPO:0005978 | |||||||||||||||||||||||||||||
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 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) |
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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) |