Hyperglycemia
Symptom Information:
Symptom ID: | HPO:0003074 | ||
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) Abnormality of blood glucose concentration(HPO:0011015) Hyperglycemia(HPO:0003074) MedDRA: |
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Database Frequency: | 37 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2 | (OMIM:615954) |
Alström syndrome | (Orphanet:64) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
DEND syndrome | (Orphanet:79134) |
DIABETES MELLITUS, INSULIN-DEPENDENT | (OMIM:222100) |
DIABETES MELLITUS, TRANSIENT NEONATAL, 1 | (OMIM:601410) |
DK1-CDG | (Orphanet:91131) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
HYPERPROINSULINEMIA | (OMIM:616214) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Leprechaunism | (Orphanet:508) |
MITCHELL-RILEY SYNDROME | (OMIM:615710) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Marden-Walker syndrome | (Orphanet:2461) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
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 9 | (OMIM:612225) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Neonatal diabetes mellitus | (Orphanet:224) |
Neonatal hemochromatosis | (Orphanet:446) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Proximal myotonic myopathy | (Orphanet:606) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SHORT syndrome | (Orphanet:3163) |
Transient neonatal diabetes mellitus | (Orphanet:99886) |