Stereotypy
Symptom Information:
Symptom ID: | HPO:0000733 | |||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||
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) |