Short attention span
Symptom Information:
Symptom ID: | HPO:0000736 | |||
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 higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Short attention span(HPO:0000736) MedDRA: |
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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) |