Impaired social interactions

Symptom Information:

Symptom ID: HPO:0000735
Synonyms:
Impaired social interaction [HPO:0000735]
Poor social interactions [HPO:0000735]
Impaired social interaction [OMIM:Impaired social interaction]
Impaired social interactions [OMIM:Impaired social interactions]
Poor social interactions [OMIM:Poor social interactions]
Poor social interaction [OMIM:Poor social interaction]
Quality:
Cross references:
OMIM: "Impaired social interaction" [OMIM:Impaired social interaction]
OMIM: "Impaired social interactions" [OMIM:Impaired social interactions]
OMIM: "Poor social interactions" [OMIM:Poor social interactions]
OMIM: "Poor social interaction" [OMIM:Poor social interaction]
Is a (Direct Parents):
HPO         Abnormal social 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 social behavior(HPO:0012433)
                         Impaired social interactions(HPO:0000735)
MedDRA:
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)