Polyphagia
Symptom Information:
Symptom ID: | HPO:0002591 | |||||||||||||||||||||||||||
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 the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Abnormal eating behavior(HPO:0100738) Polyphagia(HPO:0002591) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Appetite and general nutritional disorders(MedDRA:10003018) Appetite disorders(MedDRA:10003022) Polyphagia(HPO:0002591) Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal signs and symptoms(MedDRA:10018012) Gastrointestinal signs and symptoms NEC(MedDRA:10027678) Polyphagia(HPO:0002591) |
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Database Frequency: | 25 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
6q16 deletion syndrome | (Orphanet:171829) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
CHROMOSOME 22q13 DUPLICATION SYNDROME | (OMIM:615538) |
DIABETES MELLITUS, INSULIN-DEPENDENT | (OMIM:222100) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
FRONTOTEMPORAL DEMENTIA | (OMIM:600274) |
Frontotemporal dementia | (Orphanet:282) |
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Kleine-Levin syndrome | (Orphanet:33543) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
MACROSOMIA ADIPOSA CONGENITA | (OMIM:248100) |
OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY | (OMIM:613886) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
Obesity due to leptin receptor gene deficiency | (Orphanet:179494) |
PICK DISEASE OF BRAIN | (OMIM:172700) |
Prader-Willi syndrome | (Orphanet:739) |
Progressive non-fluent aphasia | (Orphanet:100070) |
Renal glucosuria | (Orphanet:69076) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
Weaver syndrome | (Orphanet:3447) |