Diabetes mellitus
Symptom Information:
Symptom ID: | HPO:0000819 | ||||||||||||||||||||||||
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 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) |
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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) |