Glucose intolerance
Symptom Information:
Symptom ID: | HPO:0000833 | |||||
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) Abnormal glucose tolerance(HPO:0001952) Glucose intolerance(HPO:0000833) MedDRA: |
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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) |