Poor eye contact
Symptom Information:
Symptom ID: | HPO:0000817 | ||
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) Poor eye contact(HPO:0000817) MedDRA: |
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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) |