Bipolar affective disorder

Symptom Information:

Symptom ID: HPO:0007302
Synonyms:
Bipolar disorder [HPO:0007302]
Bipolar disorder [Orphanet:43630]
Bipolar disorder (disorder) [Orphanet:43630]
Bipolar Disorder [Orphanet:43630]
Bipolar affective disorder [OMIM:Bipolar affective disorder]
Bipolar disorder [OMIM:Bipolar disorder]
Psychosis/schizophrenia/maniac disorder [Orphanet:43630]
Bipolar disorder [MedDRA:10057667]
Bipolar affective disorder [MedDRA:10057667]
Bipolar affective disorder aggr. [MedDRA:10057667]
Bipolar affective disorder aggravated [MedDRA:10057667]
Bipolar affective disorder, unspecified [MedDRA:10057667]
Bipolar disorder NEC [MedDRA:10057667]
Bipolar disorders [MedDRA:10004938]
Quality:
Cross references:
Orphanet:43630 "Psychosis/schizophrenia/maniac disorder" [Orphanet:43630]
OMIM: "Bipolar affective disorder" [OMIM:Bipolar affective disorder]
OMIM: "Bipolar disorder" [OMIM:Bipolar disorder]
UMLS:C0005586 "Bipolar Disorder" [Orphanet:43630]
Is a (Direct Parents):
HPO         Depression
MedDRA Manic and bipolar mood disorders and disturbances
Orphanet Behavioral abnormality
HPO         Mania
Orphanet Psychosis
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)
                   Mania(HPO:0100754)
                      Bipolar affective disorder(HPO:0007302)
                   Abnormal emotion/affect behavior(HPO:0100851)
                      Depression(HPO:0000716)
                         Bipolar affective disorder(HPO:0007302)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
48,XXYY syndrome (Orphanet:10)
Alström syndrome (Orphanet:64)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
CHROMOSOME 22q13 DUPLICATION SYNDROME (OMIM:615538)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
DIGEORGE SYNDROME (OMIM:188400)
Darier disease (Orphanet:218)
Gómez-López-Hernández syndrome (Orphanet:1532)
LITHIUM TRANSPORT (OMIM:152420)
MAJOR AFFECTIVE DISORDER 2 (OMIM:309200)
MELAS (Orphanet:550)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Wolfram syndrome (Orphanet:3463)