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.
Fragile X syndrome
Occasional (5-29%)
Steroid sulfatase deficiency
Occasional (5-29%)
Bardet-Biedl syndrome
Frequent (30-79%)
Tuberous sclerosis syndrome
Frequent (30-79%)
Septo-optic dysplasia sequence
Occasional (5-29%)
Juvenile polyposis syndrome
Atrophia bulborum hereditaria
Occasional (5-29%)
Adenylosuccinate lyase deficiency
Cyclical vomiting syndrome
Poisoning by fluorouracil
Occasional (5-29%)
XXXXY syndrome
Frequent (30-79%)
De Lange syndrome
Occasional (5-29%)
Autistic disorder of childhood onset
Smith-Lemli-Opitz syndrome
Frequent (30-79%)
Rubinstein-Taybi syndrome
CHARGE association
Frequent (30-79%)
Succinate-semialdehyde dehydrogenase deficiency
Cowden syndrome
Occasional (5-29%)
Glutamate formiminotransferase deficiency
Very rare (1-4%)
Cholestanol storage disease
Occasional (5-29%)
Williams syndrome
Frequent (30-79%)
Porphobilinogen synthase deficiency
Occasional (5-29%)
5p partial monosomy syndrome
Dihydrouracil dehydrogenase (NADP^+^) deficiency
Occasional (5-29%)
Steinert myotonic dystrophy syndrome
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 34883005
- UMLS CUI
- C0233639
- Fully Specified Name
- Autistic thinking (finding)
- Associated Conditions
- 25
- 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.