Attention deficit hyperactivity disorder
Symptom Information:
Symptom ID: | HPO:0007018 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Attention deficit hyperactivity disorder(HPO:0007018) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Short attention span(HPO:0000736) Attention deficit hyperactivity disorder(HPO:0007018) MedDRA: |
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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) |