Polyphagia

Symptom Information:

Symptom ID: HPO:0002591
Synonyms:
Hyperphagia [HPO:0002591]
Increased appetite [HPO:0002591]
Voracious appetite [HPO:0002591]
Increased appetite (finding) [Orphanet:43610]
Overeating (finding) [Orphanet:43610]
Excessive eating - polyphagia (finding) [Orphanet:43610]
POLYPHAGIA [HPO:0002591]
Hyperphagia [Orphanet:43610]
Hyperphagia [OMIM:Hyperphagia]
Increased appetite [OMIM:Increased appetite]
Polyphagia [OMIM:Polyphagia]
Voracious appetite [OMIM:Voracious appetite]
Bulimia/hyperphagia [Orphanet:43610]
Increased appetite [Orphanet:43610]
Increased appetite [MedDRA:10021654]
Appetite exaggerated [MedDRA:10021654]
Appetite excessive [MedDRA:10021654]
Appetite increased NOS [MedDRA:10021654]
Appetite stimulated [MedDRA:10021654]
Hyperphagia [MedDRA:10020710]
Excessive eating [MedDRA:10020710]
Markedly increased food intake [MedDRA:10020710]
Other hyperalimentation [MedDRA:10020710]
Polyphagia [MedDRA:10020710]
Markedly increased dietary intake [MedDRA:10020710]
Excessive appetite [OMIM:Excessive appetite]
Hyperphagia (deletion patients) [OMIM:Hyperphagia (deletion patients)]
Quality:
Cross references:
Orphanet:43610 "Bulimia/hyperphagia" [Orphanet:43610]
OMIM: "Hyperphagia" [OMIM:Hyperphagia]
OMIM: "Increased appetite" [OMIM:Increased appetite]
OMIM: "Polyphagia" [OMIM:Polyphagia]
OMIM: "Voracious appetite" [OMIM:Voracious appetite]
OMIM: "Excessive appetite" [OMIM:Excessive appetite]
OMIM: "Hyperphagia (deletion patients)" [OMIM:Hyperphagia (deletion patients)]
UMLS:C0020505 "POLYPHAGIA" [HPO:0002591]
UMLS:C0232461 "Increased appetite (finding)" [Orphanet:43610]
UMLS:C0020505 "Hyperphagia" [Orphanet:43610]
Is a (Direct Parents):
HPO         Abnormal eating behavior
MedDRA Appetite disorders
Orphanet Behavioral abnormality
MedDRA Gastrointestinal signs and symptoms NEC
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)
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)