Type I diabetes mellitus
Symptom Information:
Symptom ID: | HPO:0100651 | |||||||||||||||||||||||||||
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 I diabetes mellitus(HPO:0100651) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013) Abnormal glucose homeostasis(HPO:0011014) Diabetes mellitus(HPO:0000819) Type I diabetes mellitus(HPO:0100651) MedDRA: Immune system disorders(MedDRA:10021428) Autoimmunity(HPO:0002960) Endocrine autoimmune disorders(MedDRA:10003818) Type I diabetes mellitus(HPO:0100651) |
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Database Frequency: | 44 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS ANDDIABETES MELLITUS | (OMIM:616192) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Bangstad syndrome | (Orphanet:1227) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Congenital rubella syndrome | (Orphanet:290) |
Cystinosis | (Orphanet:213) |
DIABETES MELLITUS, INSULIN-DEPENDENT, 10 | (OMIM:601942) |
DIABETES MELLITUS, INSULIN-DEPENDENT, 15 | (OMIM:601666) |
DIABETES MELLITUS, INSULIN-DEPENDENT, 2 | (OMIM:125852) |
DIABETES MELLITUS, INSULIN-DEPENDENT, 20 | (OMIM:612520) |
DIABETES MELLITUS, INSULIN-DEPENDENT, 6 | (OMIM:601941) |
Faisalabad histiocytosis | (Orphanet:254707) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
H syndrome | (Orphanet:168569) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Infantile axonal neuropathy | (Orphanet:2679) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
MELAS | (Orphanet:550) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
Partial pancreatic agenesis | (Orphanet:2805) |
Pearson syndrome | (Orphanet:699) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Prader-Willi syndrome | (Orphanet:739) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Rosaï-Dorfman disease | (Orphanet:158014) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Syndromic multisystem autoimmune disease due to Itch deficiency | (Orphanet:228426) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |