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
Frequent (30-79%)
Dubowitz's syndrome
Agenesis of corpus callosum
Occasional (5-29%)
Bardet-Biedl syndrome
Occasional (5-29%)
Galactose epimerase deficiency
Always present (100%)
Crigler-Najjar syndrome, type I
Occasional (5-29%)
Coffin-Siris syndrome
Always present (100%)
Ring chromosome 22 syndrome
Frequent (30-79%)
Adenylosuccinate lyase deficiency
Mucopolysaccharidosis, MPS-III-D
Always present (100%)
Sturge-Weber sequence
Frequent (30-79%)
5-Oxoprolinase deficiency
Occasional (5-29%)
Progressive supranuclear ophthalmoplegia
Frequent (30-79%)
Ring chromosome 21 syndrome
Occasional (5-29%)
Arteriohepatic dysplasia
Always present (100%)
Poisoning by fluorouracil
Occasional (5-29%)
Greig cephalopolysyndactyly syndrome
Always present (100%)
Microtia
Frequent (30-79%)
Trisomy X syndrome
Frequent (30-79%)
Nager syndrome
Very frequent (80-99%)
De Lange syndrome
Very frequent (80-99%)
Argininosuccinate lyase deficiency
Occasional (5-29%)
Langer-Giedion syndrome
Autistic disorder of childhood onset
Rubinstein-Taybi syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 162294008
- UMLS CUI
- C0233715
- Fully Specified Name
- Has difficulty with speech (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.