Schizophrenia
Symptom Information:
Symptom ID: | HPO:0100753 | |||||||||||||||||||||||||||||||||||||||||||||
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) Schizophrenia(HPO:0100753) MedDRA: |
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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) |