Schizophrenia

Symptom Information:

Symptom ID: HPO:0100753
Synonyms:
Schizophrenia (disorder) [Orphanet:43630]
Schizophrenic disorders (disorder) [Orphanet:43630]
Schizophrenia [Orphanet:43630]
Schizophrenia [OMIM:Schizophrenia]
Psychosis/schizophrenia/maniac disorder [Orphanet:43630]
Schizophrenia [MedDRA:10039626]
Acute schizophrenia [MedDRA:10039626]
Acute schizophrenia episode [MedDRA:10039626]
Acute schizophrenic episode [MedDRA:10039626]
Acute schizophrenic episode, chronic state [MedDRA:10039626]
Acute schizophrenic episode, chronic state with acute exacerbation [MedDRA:10039626]
Acute schizophrenic episode, in remission [MedDRA:10039626]
Acute schizophrenic episode, subchronic state [MedDRA:10039626]
Acute schizophrenic episode, subchronic state with acute exacerbation [MedDRA:10039626]
Acute schizophrenic episode, unspecified state [MedDRA:10039626]
Childhood schizophrenia [MedDRA:10039626]
Chronic schizophrenia [MedDRA:10039626]
Dementia praecox [MedDRA:10039626]
Other schizophrenic psychoses [MedDRA:10039626]
Other specified types of schizophrenia [MedDRA:10039626]
Other specified types of schizophrenia, chronic state [MedDRA:10039626]
Other specified types of schizophrenia, chronic state with acute exacerbation [MedDRA:10039626]
Other specified types of schizophrenia, in remission [MedDRA:10039626]
Other specified types of schizophrenia, subchronic state [MedDRA:10039626]
Other specified types of schizophrenia, subchronic state with acute exacerbation [MedDRA:10039626]
Other specified types of schizophrenia, unspecified state [MedDRA:10039626]
Schizophrenia aggravated [MedDRA:10039626]
Schizophrenia childhood [MedDRA:10039626]
Schizophrenia exacerbated [MedDRA:10039626]
Schizophrenia NOS [MedDRA:10039626]
Schizophrenia NOS aggravated [MedDRA:10039626]
Schizophrenic disorders [MedDRA:10039626]
Schizophrenic psychoses [MedDRA:10039626]
Unspecified schizophrenia [MedDRA:10039626]
Unspecified schizophrenia, chronic state [MedDRA:10039626]
Unspecified schizophrenia, chronic state with acute exacerbation [MedDRA:10039626]
Unspecified schizophrenia, in remission [MedDRA:10039626]
Unspecified schizophrenia, subchronic state [MedDRA:10039626]
Unspecified schizophrenia, subchronic state with acute exacerbation [MedDRA:10039626]
Unspecified schizophrenia, unspecified state [MedDRA:10039626]
Schizophrenia relapse [MedDRA:10039626]
Treatment-resistant schizophrenia [MedDRA:10039626]
Schizophrenia (22% of adults) [OMIM:Schizophrenia (22% of adults)]
Schizophrenia (in some patients) [OMIM:Schizophrenia (in some patients)]
Schizophrenia (rare) [OMIM:Schizophrenia (rare)]
Quality:
Cross references:
Orphanet:43630 "Psychosis/schizophrenia/maniac disorder" [Orphanet:43630]
OMIM: "Schizophrenia" [OMIM:Schizophrenia]
OMIM: "Schizophrenia (22% of adults)" [OMIM:Schizophrenia (22% of adults)]
OMIM: "Schizophrenia (in some patients)" [OMIM:Schizophrenia (in some patients)]
OMIM: "Schizophrenia (rare)" [OMIM:Schizophrenia (rare)]
UMLS:C0036341 "Schizophrenia" [Orphanet:43630]
Is a (Direct Parents):
Orphanet Psychosis
Orphanet Behavioral abnormality
MedDRA Schizophrenia NEC
HPO         Behavioral abnormality
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)
                   Schizophrenia(HPO:0100753)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
1q21.1 microdeletion syndrome (Orphanet:250989)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
48,XXYY syndrome (Orphanet:10)
Alström syndrome (Orphanet:64)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
DIGEORGE SYNDROME (OMIM:188400)
Darier disease (Orphanet:218)
MELAS (Orphanet:550)
SCHIZOPHRENIA (OMIM:181500)
SCHIZOPHRENIA 1 (OMIM:181510)
SCHIZOPHRENIA 10 (OMIM:605419)
SCHIZOPHRENIA 15 (OMIM:613950)
SCHIZOPHRENIA 3 (OMIM:600511)
SCHIZOPHRENIA 4 (OMIM:600850)
Wilson disease (Orphanet:905)
Wolfram syndrome (Orphanet:3463)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)