Glucose intolerance

Symptom Information:

Symptom ID: HPO:0000833
Synonyms:
Impaired glucose tolerance [HPO:0000833]
Glucose intolerance [OMIM:Glucose intolerance]
Impaired glucose tolerance [OMIM:Impaired glucose tolerance]
Impaired glucose tolerance (in male patient) [OMIM:Impaired glucose tolerance (in male patient)]
Impaired glucose tolerance (in some patients) [OMIM:Impaired glucose tolerance (in some patients)]
Quality:
Cross references:
OMIM: "Glucose intolerance" [OMIM:Glucose intolerance]
OMIM: "Impaired glucose tolerance" [OMIM:Impaired glucose tolerance]
OMIM: "Impaired glucose tolerance (in male patient)" [OMIM:Impaired glucose tolerance (in male patient)]
OMIM: "Impaired glucose tolerance (in some patients)" [OMIM:Impaired glucose tolerance (in some patients)]
Is a (Direct Parents):
HPO         Abnormal glucose tolerance
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)
                Abnormal glucose tolerance(HPO:0001952)
                   Glucose intolerance(HPO:0000833)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA (OMIM:208900)
Ataxia-telangiectasia (Orphanet:100)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Cushing disease (Orphanet:96253)
ESTROGEN RESISTANCE (OMIM:615363)
Friedreich ataxia 1 (OMIM:229300)
Hemochromatosis type 3 (Orphanet:225123)
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)
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome (Orphanet:329332)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Renal cysts and diabetes syndrome (Orphanet:93111)
SHORT syndrome (Orphanet:3163)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Skeletal dysplasia - intellectual deficit (Orphanet:1436)
Williams syndrome (Orphanet:904)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)