Poor eye contact

Symptom Information:

Symptom ID: HPO:0000817
Synonyms:
Poor eye contact [OMIM:Poor eye contact]
Poor eye contact (in some patients) [OMIM:Poor eye contact (in some patients)]
Quality:
Cross references:
OMIM: "Poor eye contact" [OMIM:Poor eye contact]
OMIM: "Poor eye contact (in some patients)" [OMIM:Poor eye contact (in some patients)]
Is a (Direct Parents):
HPO         Impaired social interactions
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)
                            Poor eye contact(HPO:0000817)
MedDRA:
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
17p11.2 microduplication syndrome (Orphanet:1713)
5q14.3 microdeletion syndrome (Orphanet:228384)
Adenylosuccinate lyase deficiency (Orphanet:46)
Atypical Rett syndrome (Orphanet:3095)
D,L-2-hydroxyglutaric aciduria (Orphanet:356978)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 (OMIM:614959)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 (OMIM:615006)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Epileptic encephalopathy with global cerebral demyelination (Orphanet:353217)
Fragile X syndrome (Orphanet:908)
Gaucher disease type 2 (Orphanet:77260)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hypotonia-speech impairment-severe cognitive delay syndrome (Orphanet:371364)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit, X-linked, Cantagrel type (Orphanet:85277)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 (OMIM:615828)
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C (OMIM:615501)
Maternally-inherited Leigh syndrome (Orphanet:255210)
Monosomy 22q13 (Orphanet:48652)
PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE (OMIM:608097)
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 (OMIM:615803)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES (OMIM:612948)