Type I diabetes mellitus

Symptom Information:

Symptom ID: HPO:0100651
Synonyms:
Diabetes mellitus Type I [HPO:0100651]
Insulin-dependent diabetes mellitus [HPO:0100651]
INSULIN-DEPENDENT DIABETES MELLITUS (TYPE I) [HPO:0100651]
Juvenile diabetes mellitus [HPO:0100651]
Type I Diabetes mellitus [Orphanet:41600]
Diabetes mellitus type 1 (disorder) [Orphanet:41600]
Diabetes Mellitus, Insulin-Dependent [Orphanet:41600]
Insulin-dependent diabetes mellitus [OMIM:Insulin-dependent diabetes mellitus]
Insulin-dependent diabetes mellitus (type I) [OMIM:Insulin-dependent diabetes mellitus (type I)]
Insulin-dependent/type 1 diabetes [Orphanet:41600]
Type 1 diabetes mellitus [Orphanet:41600]
Type 1 diabetes mellitus [MedDRA:10067584]
Diabetes mellitus insulin-dependent [MedDRA:10067584]
Diabetes mellitus juvenile onset [MedDRA:10067584]
IDDM [MedDRA:10067584]
Insulin dependent diabetic [MedDRA:10067584]
Insulin-dependent diabetes mellitus [MedDRA:10067584]
Juvenile diabetes [MedDRA:10067584]
Ketosis-prone diabetes mellitus [MedDRA:10067584]
Type I diabetes mellitus [MedDRA:10067584]
Type I diabetes mellitus without mention of complication [MedDRA:10067584]
Diabetes mellitus, insulin-dependent [OMIM:Diabetes mellitus, insulin-dependent]
Diabetes mellitus, insulin-dependent (1 patient) [OMIM:Diabetes mellitus, insulin-dependent (1 patient)]
Diabetes mellitus, type 1 (rare) [OMIM:Diabetes mellitus, type 1 (rare)]
Insulin dependent diabetes mellitus [OMIM:Insulin dependent diabetes mellitus]
Insulin- dependent diabetes mellitus [OMIM:Insulin- dependent diabetes mellitus]
Insulin-dependent diabetes mellitus (onset in infancy) [OMIM:Insulin-dependent diabetes mellitus (onset in infancy)]
Quality:
Cross references:
Orphanet:41600 "Insulin-dependent/type 1 diabetes" [Orphanet:41600]
OMIM: "Insulin-dependent diabetes mellitus" [OMIM:Insulin-dependent diabetes mellitus]
OMIM: "Insulin-dependent diabetes mellitus (type I)" [OMIM:Insulin-dependent diabetes mellitus (type I)]
OMIM: "Diabetes mellitus, insulin-dependent" [OMIM:Diabetes mellitus, insulin-dependent]
OMIM: "Diabetes mellitus, insulin-dependent (1 patient)" [OMIM:Diabetes mellitus, insulin-dependent (1 patient)]
OMIM: "Diabetes mellitus, type 1 (rare)" [OMIM:Diabetes mellitus, type 1 (rare)]
OMIM: "Insulin dependent diabetes mellitus" [OMIM:Insulin dependent diabetes mellitus]
OMIM: "Insulin- dependent diabetes mellitus" [OMIM:Insulin- dependent diabetes mellitus]
OMIM: "Insulin-dependent diabetes mellitus (onset in infancy)" [OMIM:Insulin-dependent diabetes mellitus (onset in infancy)]
UMLS:C0011854 "Diabetes Mellitus, Insulin-Dependent" [Orphanet:41600]
Is a (Direct Parents):
Orphanet Diabetes mellitus
MedDRA Endocrine autoimmune disorders
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 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)
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)