Hyperglycemia

Symptom Information:

Symptom ID: HPO:0003074
Synonyms:
Hyperglycemia [OMIM:Hyperglycemia]
Quality:
Cross references:
OMIM: "Hyperglycemia" [OMIM:Hyperglycemia]
UMLS:C0020456 "Hyperglycemia" [HPO:0003074]
Is a (Direct Parents):
HPO         Abnormality of blood glucose concentration
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:
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)