Impaired social interactions
Symptom Information:
Symptom ID: | HPO:0000735 | ||||||
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) Abnormal emotion/affect behavior(HPO:0100851) Abnormal social behavior(HPO:0012433) Impaired social interactions(HPO:0000735) MedDRA: |
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Database Frequency: | 20 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
15q11q13 microduplication syndrome | (Orphanet:238446) |
1p36 deletion syndrome | (Orphanet:1606) |
ALG11-CDG | (Orphanet:280071) |
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1 | (OMIM:608638) |
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2 | (OMIM:608631) |
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 | (OMIM:300494) |
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 | (OMIM:300497) |
AUTISM | (OMIM:209850) |
AUTISM, SUSCEPTIBILITY TO, 3 | (OMIM:608049) |
AUTISM, SUSCEPTIBILITY TO, 8 | (OMIM:607373) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 | (OMIM:300425) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 | (OMIM:300495) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 | (OMIM:300496) |
Classical phenylketonuria | (Orphanet:79254) |
Cortical dysplasia - focal epilepsy syndrome | (Orphanet:163681) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Monosomy 22q13 | (Orphanet:48652) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
X-linked creatine transporter deficiency | (Orphanet:52503) |