Impulsivity

Symptom Information:

Symptom ID: HPO:0100710
Synonyms:
Impulsivity [OMIM:Impulsivity]
Quality:
Cross references:
OMIM: "Impulsivity" [OMIM:Impulsivity]
Is a (Direct Parents):
HPO         Abnormal aggressive, impulsive or violent behavior
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)
                   Abnormal emotion/affect behavior(HPO:0100851)
                      Abnormal aggressive, impulsive or violent behavior(HPO:0006919)
                         Impulsivity(HPO:0100710)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Adenylosuccinate lyase deficiency (Orphanet:46)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
CHROMOSOME Xp22 DELETION SYNDROME (OMIM:300830)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
FRAXE intellectual deficit (Orphanet:100973)
Glycine encephalopathy (Orphanet:407)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:604321)
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:614852)
MONOAMINE OXIDASE A (OMIM:309850)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
NEUROPATHY, HEREDITARY SENSORY, TYPE IE (OMIM:614116)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Wolfram syndrome 1 (OMIM:222300)