Short attention span

Symptom Information:

Symptom ID: HPO:0000736
Synonyms:
Poor attention span [HPO:0000736]
Poor attention span [OMIM:Poor attention span]
Short attention span [OMIM:Short attention span]
Quality:
Cross references:
OMIM: "Poor attention span" [OMIM:Poor attention span]
OMIM: "Short attention span" [OMIM:Short attention span]
Is a (Direct Parents):
HPO         Behavioral abnormality
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)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

2q23.1 microdeletion syndrome (Orphanet:228402)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
Adenylosuccinate lyase deficiency (Orphanet:46)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Distal monosomy 10q (Orphanet:96148)
Dubowitz syndrome (Orphanet:235)
Growth delay due to insulin-like growth factor type 1 deficiency (Orphanet:73272)
Lesch-Nyhan syndrome (Orphanet:510)
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3 (OMIM:608443)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
Monosomy 5p (Orphanet:281)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)