Stereotypy

Symptom Information:

Symptom ID: HPO:0000733
Synonyms:
Perseverative behavior [HPO:0000733]
Stereotyped behavior [HPO:0000733]
Stereotyped, repetitive behaviour [HPO:0000733]
Stereotypic behaviors [HPO:0000733]
Stereotypical motor behaviors [HPO:0000733]
Stereotypy [HPO:0000733]
Sterotyped behavior [HPO:0000733]
Stereotypy [Orphanet:43280]
Stereotyped routines (finding) [Orphanet:43280]
Stereotypy habit disorder (disorder) [Orphanet:43280]
Stereotyped Behavior [Orphanet:43280]
Stereotypic Movement Disorder [Orphanet:43280]
Perseverative behavior [OMIM:Perseverative behavior]
Stereotyped behavior [OMIM:Stereotyped behavior]
Stereotypic behavior [OMIM:Stereotypic behavior]
Stereotypic behaviors [OMIM:Stereotypic behaviors]
Stereotypical motor behaviors [OMIM:Stereotypical motor behaviors]
Tics/stereotypias [Orphanet:43280]
Stereotypy [MedDRA:10042008]
Mannerism [MedDRA:10042008]
Stereotyped repetitive movements [MedDRA:10042008]
Stereotypic movement disorder [MedDRA:10042008]
Stereotypic movement disorder (of childhood) [MedDRA:10042008]
Stereotypy/habit disorder [MedDRA:10042008]
Punding [MedDRA:10042008]
Stereotyped behaviors [OMIM:Stereotyped behaviors]
Stereotypic behavior (1 patient) [OMIM:Stereotypic behavior (1 patient)]
Stereotypic behaviors (hand-washing movements, head-banging) [OMIM:Stereotypic behaviors (hand-washing movements, head-banging)]
Stereotypic behaviors (tantrums, aggressiveness) [OMIM:Stereotypic behaviors (tantrums, aggressiveness)]
Quality:
Cross references:
Orphanet:43280 "Tics/stereotypias" [Orphanet:43280]
OMIM: "Perseverative behavior" [OMIM:Perseverative behavior]
OMIM: "Stereotyped behavior" [OMIM:Stereotyped behavior]
OMIM: "Stereotypic behavior" [OMIM:Stereotypic behavior]
OMIM: "Stereotypic behaviors" [OMIM:Stereotypic behaviors]
OMIM: "Stereotypical motor behaviors" [OMIM:Stereotypical motor behaviors]
OMIM: "Stereotyped behaviors" [OMIM:Stereotyped behaviors]
OMIM: "Stereotypic behavior (1 patient)" [OMIM:Stereotypic behavior (1 patient)]
OMIM: "Stereotypic behaviors (hand-washing movements, head-banging)" [OMIM:Stereotypic behaviors (hand-washing movements, head-banging)]
OMIM: "Stereotypic behaviors (tantrums, aggressiveness)" [OMIM:Stereotypic behaviors (tantrums, aggressiveness)]
UMLS:C0038271 "Stereotyped Behavior" [Orphanet:43280]
UMLS:C0038273 "Stereotypic Movement Disorder" [Orphanet:43280]
Is a (Direct Parents):
HPO         Punding
MedDRA Stereotypies and automatisms
HPO         Behavioral abnormality
Orphanet Abnormality of movement
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)
                   Stereotypy(HPO:0000733)
MedDRA:
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

14q12 microdeletion syndrome (Orphanet:261144)
15q11q13 microduplication syndrome (Orphanet:238446)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
17p11.2 microduplication syndrome (Orphanet:1713)
1p36 deletion syndrome (Orphanet:1606)
22q11.2 microduplication syndrome (Orphanet:1727)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q37 microdeletion syndrome (Orphanet:1001)
3q29 microdeletion syndrome (Orphanet:65286)
48,XXYY syndrome (Orphanet:10)
4q21 microdeletion syndrome (Orphanet:238750)
5p13 microduplication syndrome (Orphanet:329802)
5q14.3 microdeletion syndrome (Orphanet:228384)
AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:612069)
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1 (OMIM:608638)
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2 (OMIM:608631)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (OMIM:300494)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (OMIM:300497)
AUTISM (OMIM:209850)
AUTISM, SUSCEPTIBILITY TO, 3 (OMIM:608049)
AUTISM, SUSCEPTIBILITY TO, 8 (OMIM:607373)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 (OMIM:300425)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 (OMIM:300495)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 (OMIM:300496)
Adenylosuccinate lyase deficiency (Orphanet:46)
Atypical Rett syndrome (Orphanet:3095)
Behavioral variant of frontotemporal dementia (Orphanet:275864)
Cystinosis (Orphanet:213)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Frontotemporal dementia (Orphanet:282)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
Hyperprolinemia type 1 (Orphanet:419)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Kleefstra syndrome (Orphanet:261494)
Leigh syndrome (Orphanet:506)
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES (OMIM:613670)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 (OMIM:615541)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 (OMIM:615637)
MENTAL RETARDATION, X-LINKED 72 (OMIM:300271)
MGAT2-CDG (Orphanet:79329)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Monosomy 5p (Orphanet:281)
Mowat-Wilson syndrome (Orphanet:2152)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Norrie disease (Orphanet:649)
Oculocerebrorenal syndrome (Orphanet:534)
PICK DISEASE OF BRAIN (OMIM:172700)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Rett syndrome (Orphanet:778)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Smith-Magenis syndrome (Orphanet:819)
Transketolase deficiency (ORPHA:488618)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wolfram syndrome 1 (OMIM:222300)
X-linked creatine transporter deficiency (Orphanet:52503)