Diabetes mellitus

Symptom Information:

Symptom ID: HPO:0000819
Synonyms:
Diabetes mellitus (disorder) [Orphanet:41570]
Diabetes Mellitus [Orphanet:41570]
Diabetes mellitus [OMIM:Diabetes mellitus]
Diabetes mellitus [Orphanet:41570]
Diabetes mellitus [MedDRA:10012601]
Diabetes [MedDRA:10012601]
Diabetes mellitus aggravated [MedDRA:10012601]
Diabetes mellitus exacerbated [MedDRA:10012601]
Diabetes mellitus NOS [MedDRA:10012601]
Diabetes mellitus precipitated [MedDRA:10012601]
Diabetes mellitus reactivated [MedDRA:10012601]
Diabetes mellitus without mention of complication [MedDRA:10012601]
Diabetes reactivated [MedDRA:10012601]
Diabetes steroid-induced [MedDRA:10012601]
Diabetic [MedDRA:10012601]
Worsening of diabetes [MedDRA:10012601]
Post transplant diabetes mellitus [MedDRA:10012601]
Diabetes mellitus progression [MedDRA:10012601]
Diabetes (in affected males) [OMIM:Diabetes (in affected males)]
Diabetes (may develop later in life) [OMIM:Diabetes (may develop later in life)]
Diabetes mellitus (NIDDM) [OMIM:Diabetes mellitus (NIDDM)]
Diabetes mellitus (in some patients) [OMIM:Diabetes mellitus (in some patients)]
Diabetes mellitus (less common) [OMIM:Diabetes mellitus (less common)]
Diabetes mellitus (incl subtypes) [MedDRA:10012602]
Quality:
Cross references:
Orphanet:41570 "Diabetes mellitus" [Orphanet:41570]
OMIM: "Diabetes mellitus" [OMIM:Diabetes mellitus]
OMIM: "Diabetes (in affected males)" [OMIM:Diabetes (in affected males)]
OMIM: "Diabetes (may develop later in life)" [OMIM:Diabetes (may develop later in life)]
OMIM: "Diabetes mellitus (NIDDM)" [OMIM:Diabetes mellitus (NIDDM)]
OMIM: "Diabetes mellitus (in some patients)" [OMIM:Diabetes mellitus (in some patients)]
OMIM: "Diabetes mellitus (less common)" [OMIM:Diabetes mellitus (less common)]
UMLS:C0011849 "Diabetes Mellitus" [Orphanet:41570]
Is a (Direct Parents):
HPO         Abnormality of the endocrine system
MedDRA Glucose metabolism disorders (incl diabetes mellitus)
Orphanet Anomaly of pancreatic hormones
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)
                Diabetes mellitus(HPO:0000819)
       Abnormality of the endocrine system(HPO:0000818)
          Diabetes mellitus(HPO:0000819)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424)
       Diabetes mellitus(HPO:0000819)
Database Frequency: 131 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
17q12 microdeletion syndrome (Orphanet:261265)
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:614613)
ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
ATAXIA-TELANGIECTASIA (OMIM:208900)
Aceruloplasminemia (Orphanet:48818)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acromegaly (Orphanet:963)
Alexander disease (Orphanet:58)
Ataxia with vitamin E deficiency (Orphanet:96)
Ataxia-telangiectasia (Orphanet:100)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Autosomal dominant hyperinsulinism due to SUR1 deficiency (Orphanet:276575)
Autosomal recessive hyperinsulinism due to SUR1 deficiency (Orphanet:79643)
BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY (OMIM:211369)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Beta-thalassemia major (Orphanet:231214)
Bullous pemphigoid (Orphanet:703)
Buschke-Ollendorff syndrome (Orphanet:1306)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED (OMIM:302900)
CRANIAL NERVES, RECURRENT PARESIS OF (OMIM:218200)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Castleman disease (Orphanet:160)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
DEND syndrome (Orphanet:79134)
DIABETES MELLITUS, INSULIN-DEPENDENT (OMIM:222100)
DIABETES MELLITUS, INSULIN-DEPENDENT, 10 (OMIM:601942)
DIABETES MELLITUS, INSULIN-DEPENDENT, 6 (OMIM:601941)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency (Orphanet:276598)
Dyskeratosis congenita (Orphanet:1775)
EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL (OMIM:129840)
Erythrokeratodermia variabilis (Orphanet:317)
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG (OMIM:616026)
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA (OMIM:229310)
Familial Dupuytren contracture (Orphanet:79142)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Friedreich ataxia 1 (OMIM:229300)
Friedreich ataxia 2 (OMIM:601992)
Good syndrome (Orphanet:169105)
Growth hormone insensitivity syndrome (Orphanet:181393)
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA (OMIM:610628)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hereditary chronic pancreatitis (Orphanet:676)
Holoprosencephaly (Orphanet:2162)
Hyperinsulinism due to glucokinase deficiency (Orphanet:79299)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
IMMUNODEFICIENCY 31C (OMIM:614162)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Johanson-Blizzard syndrome (Orphanet:2315)
Kearns-Sayre syndrome (Orphanet:480)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
Lymphedema - distichiasis (Orphanet:33001)
MELAS (Orphanet:550)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
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 2 (OMIM:125851)
Morgagni-Stewart-Morel syndrome (Orphanet:77296)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus (Orphanet:2579)
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys (Orphanet:79118)
Neutral lipid storage disease (Orphanet:165)
Neutral lipid storage myopathy (Orphanet:98908)
Norrie disease (Orphanet:649)
OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE (OMIM:602475)
PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT (OMIM:614674)
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION (OMIM:172500)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
PREMATURE AGING SYNDROME, OKAMOTO TYPE (OMIM:601811)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Pancreatic adenoma (Orphanet:93292)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Partial acquired lipodystrophy (Orphanet:79087)
Partial pancreatic agenesis (Orphanet:2805)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Preaxial polydactyly of toes (Orphanet:295006)
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome (Orphanet:306558)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Proximal myotonic myopathy (Orphanet:606)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Rabson-Mendenhall syndrome (Orphanet:769)
Ramon syndrome (Orphanet:3019)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renpenning syndrome (Orphanet:3242)
Rosaï-Dorfman disease (Orphanet:158014)
SHORT syndrome (Orphanet:3163)
SPLENOPORTAL VASCULAR ANOMALIES (OMIM:271500)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Steinert myotonic dystrophy (Orphanet:273)
Stimmler syndrome (Orphanet:3199)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Transketolase deficiency (ORPHA:488618)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome 2 (OMIM:604928)
Wolfram syndrome, mitochondrial form (OMIM:598500)
Wolfram-like syndrome (ORPHA:411590)
Woodhouse-Sakati syndrome (Orphanet:3464)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)