Hyperactivity
Symptom Information:
Symptom ID: | HPO:0000752 | ||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||
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 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) |
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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) |