Hyperactivity

Symptom Information:

Symptom ID: HPO:0000752
Synonyms:
Hyperactive behavior [HPO:0000752]
Hyperactive behavior (finding) [Orphanet:43540]
Hyper [HPO:0000752]
Hyperactive behavior [Orphanet:43540]
Hyperactive behavior [OMIM:Hyperactive behavior]
Hyperactivity [OMIM:Hyperactivity]
Hyperactivity/attention deficit [Orphanet:43540]
Hyperkinesia [Orphanet:43540]
Hyperkinesia [MedDRA:10020651]
Hyperkinesis [MedDRA:10020651]
Hyperkinetic reaction [MedDRA:10020651]
Attention deficit-hyperactivity [OMIM:Attention deficit-hyperactivity]
Hyperactivity (if left untreated) [OMIM:Hyperactivity (if left untreated)]
Hyperactivity (reported in 1 patient) [OMIM:Hyperactivity (reported in 1 patient)]
Quality:
Cross references:
Orphanet:43540 "Hyperactivity/attention deficit" [Orphanet:43540]
OMIM: "Hyperactive behavior" [OMIM:Hyperactive behavior]
OMIM: "Hyperactivity" [OMIM:Hyperactivity]
OMIM: "Attention deficit-hyperactivity" [OMIM:Attention deficit-hyperactivity]
OMIM: "Hyperactivity (if left untreated)" [OMIM:Hyperactivity (if left untreated)]
OMIM: "Hyperactivity (reported in 1 patient)" [OMIM:Hyperactivity (reported in 1 patient)]
UMLS:C0424295 "Hyper" [HPO:0000752]
UMLS:C0424295 "Hyperactive behavior" [Orphanet:43540]
Is a (Direct Parents):
HPO         Abnormality of movement
Orphanet Functional anomalies of the nervous system
MedDRA Dyskinesias and movement disorders NEC
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 movement(HPO:0100022)
                Hyperactivity(HPO:0000752)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dyskinesias and movement disorders NEC(MedDRA:10013929)
          Hyperactivity(HPO:0000752)
Database Frequency: 140 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microdeletion syndrome (Orphanet:276413)
15q13.3 microdeletion syndrome (Orphanet:199318)
15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microduplication syndrome (Orphanet:261204)
16p13.11 microduplication syndrome (Orphanet:261243)
17p11.2 microduplication syndrome (Orphanet:1713)
17q21.31 microduplication syndrome (Orphanet:217340)
19p13.12 microdeletion syndrome (Orphanet:254346)
1q21.1 microdeletion syndrome (Orphanet:250989)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
22q11.2 microduplication syndrome (Orphanet:1727)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
3q29 microdeletion syndrome (Orphanet:65286)
4-hydroxybutyric aciduria (Orphanet:22)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
6q16 deletion syndrome (Orphanet:171829)
8p23.1 microdeletion syndrome (Orphanet:251071)
8q12 microduplication syndrome (Orphanet:228399)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:614613)
ATTENTION DEFICIT-HYPERACTIVITY DISORDER (OMIM:143465)
Aarskog-Scott syndrome (Orphanet:915)
Adenylosuccinate lyase deficiency (Orphanet:46)
Angelman syndrome (Orphanet:72)
Argininemia (Orphanet:90)
Autosomal dominant spastic paraplegia type 29 (Orphanet:101009)
Bardet-Biedl syndrome 2 (OMIM:615981)
Beta-mannosidosis (Orphanet:118)
CHARGE syndrome (Orphanet:138)
CK syndrome (Orphanet:251383)
Cabezas syndrome (Orphanet:85293)
Carpenter-Waziri syndrome (Orphanet:93973)
Choreoacanthocytosis (Orphanet:2388)
Christianson syndrome (Orphanet:85278)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Classical phenylketonuria (Orphanet:79254)
Cornelia de Lange syndrome (Orphanet:199)
Cortical dysplasia - focal epilepsy syndrome (Orphanet:163681)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Dihydropyrimidine dehydrogenase deficiency (Orphanet:1675)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal 7q11.23 microdeletion syndrome (Orphanet:254351)
Distal 7q11.23 microduplication syndrome (Orphanet:261102)
Distal monosomy 10q (Orphanet:96148)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Dubowitz syndrome (Orphanet:235)
Dyggve-Melchior-Clausen disease (Orphanet:239)
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY (OMIM:615924)
FRAXE intellectual deficit (Orphanet:100973)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Floating-Harbor syndrome (Orphanet:2044)
Fragile X syndrome (Orphanet:908)
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:275000)
Glycine encephalopathy (Orphanet:407)
Growth delay due to insulin-like growth factor type 1 deficiency (Orphanet:73272)
Gómez-López-Hernández syndrome (Orphanet:1532)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Holmes-Gang syndrome (Orphanet:93970)
Hyperprolinemia type 1 (Orphanet:419)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficiency - hypotonia - spasticity - sleep disorder (Orphanet:356996)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
Intellectual deficit, X-linked, Cantagrel type (Orphanet:85277)
Jacobsen syndrome (Orphanet:2308)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Juberg-Marsidi syndrome (Orphanet:93972)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Legius syndrome (Orphanet:137605)
MEHMO syndrome (Orphanet:85282)
MELAS (Orphanet:550)
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES (OMIM:613670)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 (OMIM:613192)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3 (OMIM:608443)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 (OMIM:615541)
MENTAL RETARDATION, X-LINKED 101 (OMIM:300928)
MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MENTAL RETARDATION, X-LINKED 72 (OMIM:300271)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:608716)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 (OMIM:615824)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome (Orphanet:558)
Maternal hyperphenylalaninemia (Orphanet:2209)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephaly - seizures - developmental delay (Orphanet:228418)
Monosomy 5p (Orphanet:281)
Monosomy 9q22.3 (Orphanet:77301)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 3 (Orphanet:581)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Neurofibromatosis type 1 (Orphanet:636)
Neurological conditions associated with aminoacylase 1 deficiency (Orphanet:137754)
Nijmegen breakage syndrome (Orphanet:647)
Non-polyposis Turcot syndrome (Orphanet:99817)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Norrie disease (Orphanet:649)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculocerebrorenal syndrome (Orphanet:534)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Phenylketonuria (Orphanet:716)
Proximal 16p11.2 microdeletion syndrome (Orphanet:261197)
Rabies (Orphanet:770)
Recessive X-linked ichthyosis (Orphanet:461)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SECKEL SYNDROME 1 (OMIM:210600)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Schwartz-Jampel syndrome (Orphanet:800)
Seckel syndrome (Orphanet:808)
Severe combined immunodeficiency due to CORO1A deficiency (Orphanet:228003)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Sturge-Weber syndrome (Orphanet:3205)
Syndromic X-linked ichthyosis (Orphanet:281090)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Testotoxicosis (Orphanet:3000)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Trisomy X (Orphanet:3375)
Williams syndrome (Orphanet:904)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)