Attention deficit hyperactivity disorder

Symptom Information:

Symptom ID: HPO:0007018
Synonyms:
Attention deficit [HPO:0007018]
Attention deficit disorder [HPO:0007018]
Attention deficit-hyperactivity disorder [HPO:0007018]
Attention deficits [HPO:0007018]
Childhood attention deficit/hyperactivity disorder [HPO:0007018]
Attention deficit hyperactivity disorder, predominantly hyperactive impulsive type (disorder) [Orphanet:43540]
Attention deficit hyperactivity disorder, predominantly inattentive type (disorder) [Orphanet:43540]
Attention deficit hyperactivity disorder (disorder) [Orphanet:43540]
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type [Orphanet:43540]
Attention Deficit Disorder [Orphanet:43540]
Attention deficit hyperactivity disorder [Orphanet:43540]
Attention deficit [OMIM:Attention deficit]
Attention deficit disorder [OMIM:Attention deficit disorder]
Attention deficit hyperactivity disorder [OMIM:Attention deficit hyperactivity disorder]
Attention deficit-hyperactivity disorder [OMIM:Attention deficit-hyperactivity disorder]
Attention deficits [OMIM:Attention deficits]
Childhood attention deficit/hyperactivity disorder [OMIM:Childhood attention deficit/hyperactivity disorder]
Hyperactivity/attention deficit [Orphanet:43540]
Attention deficit/hyperactivity disorder [Orphanet:43540]
Attention deficit disorder [Orphanet:43540]
Attention deficit/hyperactivity disorder [MedDRA:10003736]
ADD [MedDRA:10003736]
ADDH [MedDRA:10003736]
Attention deficit disorder [MedDRA:10003736]
Attention deficit disorder of childhood [MedDRA:10003736]
Attention deficit disorder of childhood with hyperactivity [MedDRA:10003736]
Attention deficit disorder of childhood without mention of hyperactivity [MedDRA:10003736]
Attention deficit-hyperactivity disorder [MedDRA:10003736]
Attention deficit/hyperactivity disorder NOS [MedDRA:10003736]
Hyperactive child syndrome [MedDRA:10003736]
Hyperkinesis of childhood with developmental delay [MedDRA:10003736]
Hyperkinetic conduct disorder of childhood [MedDRA:10003736]
Hyperkinetic syndrome [MedDRA:10003736]
Hyperkinetic syndrome of childhood [MedDRA:10003736]
Other specified manifestations of hyperkinetic syndrome of childhood [MedDRA:10003736]
Overactive child [MedDRA:10003736]
Syndrome hyperkinetic [MedDRA:10003736]
Unspecified hyperkinetic syndrome of childhood [MedDRA:10003736]
Hyperactivity syndrome aggravated [MedDRA:10003736]
ADHD [MedDRA:10003736]
ADHD, combined type [MedDRA:10003736]
ADHD, predominantly hyperactive-impulsive type [MedDRA:10003736]
ADHD, predominantly inattentive type [MedDRA:10003736]
Attention deficit disorder (in those who stop treatment) [OMIM:Attention deficit disorder (in those who stop treatment)]
Attention deficit hyperactivity disorder (ADHD) [OMIM:Attention deficit hyperactivity disorder (ADHD)]
Attention deficit-hyperactivity [OMIM:Attention deficit-hyperactivity]
Attention deficit-hyperactivity disorder (3 patients) [OMIM:Attention deficit-hyperactivity disorder (3 patients)]
Attention deficit-hyperactivity disorder (CVS+) [OMIM:Attention deficit-hyperactivity disorder (CVS+)]
Attention deficits (in some patients) [OMIM:Attention deficits (in some patients)]
Attention-deficit disorder [OMIM:Attention-deficit disorder]
Attention-deficit hyperactivity disorder (33%) [OMIM:Attention-deficit hyperactivity disorder (33%)]
Attention-deficit/hyperactivity disorder (1/4 patients) [OMIM:Attention-deficit/hyperactivity disorder (1/4 patients)]
Quality:
Cross references:
Orphanet:43540 "Hyperactivity/attention deficit" [Orphanet:43540]
OMIM: "Attention deficit" [OMIM:Attention deficit]
OMIM: "Attention deficit disorder" [OMIM:Attention deficit disorder]
OMIM: "Attention deficit hyperactivity disorder" [OMIM:Attention deficit hyperactivity disorder]
OMIM: "Attention deficit-hyperactivity disorder" [OMIM:Attention deficit-hyperactivity disorder]
OMIM: "Attention deficits" [OMIM:Attention deficits]
OMIM: "Childhood attention deficit/hyperactivity disorder" [OMIM:Childhood attention deficit/hyperactivity disorder]
OMIM: "Attention deficit disorder (in those who stop treatment)" [OMIM:Attention deficit disorder (in those who stop treatment)]
OMIM: "Attention deficit hyperactivity disorder (ADHD)" [OMIM:Attention deficit hyperactivity disorder (ADHD)]
OMIM: "Attention deficit-hyperactivity" [OMIM:Attention deficit-hyperactivity]
OMIM: "Attention deficit-hyperactivity disorder (3 patients)" [OMIM:Attention deficit-hyperactivity disorder (3 patients)]
OMIM: "Attention deficit-hyperactivity disorder (CVS+)" [OMIM:Attention deficit-hyperactivity disorder (CVS+)]
OMIM: "Attention deficits (in some patients)" [OMIM:Attention deficits (in some patients)]
OMIM: "Attention-deficit disorder" [OMIM:Attention-deficit disorder]
OMIM: "Attention-deficit hyperactivity disorder (33%)" [OMIM:Attention-deficit hyperactivity disorder (33%)]
OMIM: "Attention-deficit/hyperactivity disorder (1/4 patients)" [OMIM:Attention-deficit/hyperactivity disorder (1/4 patients)]
UMLS:C0339002 "Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type" [Orphanet:43540]
UMLS:C0041671 "Attention Deficit Disorder" [Orphanet:43540]
UMLS:C1263846 "Attention deficit hyperactivity disorder" [Orphanet:43540]
Is a (Direct Parents):
HPO         Short attention span
Orphanet Functional anomalies of the nervous system
HPO         Hyperactivity
Orphanet Hyperactivity
MedDRA Attention deficit and disruptive behaviour disorders
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)
                   Short attention span(HPO:0000736)
                      Attention deficit hyperactivity disorder(HPO:0007018)
             Abnormality of movement(HPO:0100022)
                Hyperactivity(HPO:0000752)
                   Attention deficit hyperactivity disorder(HPO:0007018)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17p11.2 microduplication syndrome (Orphanet:1713)
17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
2-aminoadipic 2-oxoadipic aciduria (Orphanet:79154)
22q11.2 deletion syndrome (Orphanet:567)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3q13 microdeletion syndrome (Orphanet:1621)
48,XXYY syndrome (Orphanet:10)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
ATTENTION DEFICIT-HYPERACTIVITY DISORDER (OMIM:143465)
Adrenomyeloneuropathy (Orphanet:139399)
Argininosuccinic aciduria (Orphanet:23)
Bardet-Biedl syndrome 10 (OMIM:615987)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
CHROMOSOME Xp22 DELETION SYNDROME (OMIM:300830)
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA (OMIM:614306)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Classical phenylketonuria (Orphanet:79254)
DIGEORGE SYNDROME (OMIM:188400)
Duchenne muscular dystrophy (Orphanet:98896)
Epileptic encephalopathy with continuous spike-and-wave during sleep (Orphanet:725)
GILLES DE LA TOURETTE SYNDROME (OMIM:137580)
Generalized resistance to thyroid hormone (Orphanet:3221)
Hyperlysinemia, type I (OMIM:238700)
Landau-Kleffner syndrome (Orphanet:98818)
Legius syndrome (Orphanet:137605)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 (OMIM:616078)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 (OMIM:616311)
MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:608716)
Maternal hyperphenylalaninemia (Orphanet:2209)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Phenylketonuria (Orphanet:716)
Prader-Willi syndrome (Orphanet:739)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Rolandic epilepsy - speech dyspraxia (Orphanet:163721)
Saccharopinuria (Orphanet:3124)
Schilbach-Rott syndrome (Orphanet:2353)
Severe combined immunodeficiency due to CORO1A deficiency (Orphanet:228003)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Sialuria (Orphanet:3166)
Spinocerebellar ataxia type 14 (Orphanet:98763)
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT (OMIM:188570)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Transketolase deficiency (ORPHA:488618)
Tuberous sclerosis (Orphanet:805)
Tyrosinemia type 3 (Orphanet:69723)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
X-linked creatine transporter deficiency (Orphanet:52503)