Obsessive-compulsive behavior
Symptom Information:
Symptom ID: | HPO:0000722 | |||||||||||||||||||||||||
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) Obsessive-compulsive behavior(HPO:0000722) MedDRA: |
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Database Frequency: | 35 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q21.31 microduplication syndrome | (Orphanet:217340) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
2q37 microdeletion syndrome | (Orphanet:1001) |
5p13 microduplication syndrome | (Orphanet:329802) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 15q11.2 DELETION SYNDROME | (OMIM:615656) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cornelia de Lange syndrome | (Orphanet:199) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
FRAXE intellectual deficit | (Orphanet:100973) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GILLES DE LA TOURETTE SYNDROME | (OMIM:137580) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
Kleefstra syndrome | (Orphanet:261494) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 | (OMIM:615761) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Myoclonus-dystonia syndrome | (Orphanet:36899) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
OBSESSIVE-COMPULSIVE DISORDER | (OMIM:164230) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Phenylketonuria | (Orphanet:716) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Steinert myotonic dystrophy | (Orphanet:273) |
TRICHOTILLOMANIA | (OMIM:613229) |
Transketolase deficiency | (ORPHA:488618) |
Williams syndrome | (Orphanet:904) |
Wolfram syndrome 1 | (OMIM:222300) |