Language impairment
Symptom Information:
Symptom ID: | HPO:0002463 | ||||
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 higher mental function(HPO:0011446) Neurological speech impairment(HPO:0002167) Language impairment(HPO:0002463) MedDRA: |
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Database Frequency: | 15 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
FRONTOTEMPORAL DEMENTIA | (OMIM:600274) |
Frontotemporal dementia | (Orphanet:282) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
Hemolytic anemia due to adenylate kinase deficiency | (Orphanet:86817) |
Hurler syndrome | (Orphanet:93473) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 | (OMIM:615074) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 5 | (OMIM:612621) |
PICK DISEASE OF BRAIN | (OMIM:172700) |
POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE | (OMIM:615752) |
SPECIFIC LANGUAGE IMPAIRMENT 1 | (OMIM:606711) |
SPECIFIC LANGUAGE IMPAIRMENT 2 | (OMIM:606712) |
SPECIFIC LANGUAGE IMPAIRMENT 5 | (OMIM:615432) |