Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Tuberous sclerosis syndrome
Frequent (30-79%)
Metachromatic leukodystrophy, adult type
Frequent (30-79%)
Metachromatic leukodystrophy, congenital type
Occasional (5-29%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Metachromatic leukodystrophy, late infantile type
Occasional (5-29%)
Childhood absence epilepsy
Occasional (5-29%)
Williams syndrome
Very frequent (80-99%)
Niemann-Pick disease, type C
Occasional (5-29%)
Dihydrouracil dehydrogenase (NADP^+^) deficiency
Occasional (5-29%)
XXXY syndrome
Occasional (5-29%)
Hereditary geniospasm
Occasional (5-29%)
Non-progressive cerebellar ataxia with intellectual disability
Frequent (30-79%)
11q22.2q22.3 microdeletion syndrome
Occasional (5-29%)
FG syndrome type 1
Occasional (5-29%)
Congenital infiltrating lipomatosis of face
Occasional (5-29%)
SOX5 haploinsufficiency syndrome
Occasional (5-29%)
2-methyl-3-hydroxybutyric aciduria
Occasional (5-29%)
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 1141958003
- UMLS CUI
- C4021087
- Fully Specified Name
- Abnormal social behavior (finding)
- Associated Conditions
- 18
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.