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.
Gilles de la Tourette's syndrome
Mietens syndrome
Very frequent (80-99%)
Arthrochalasis multiplex congenita
Very frequent (80-99%)
Hyperammonemia, type III
Very rare (1-4%)
5p partial monosomy syndrome
Leucocyte adhesion deficiency - type 2
Frequent (30-79%)
Encephalocraniocutaneous lipomatosis
Frequent (30-79%)
Osteopathia striata with cranial sclerosis
Occasional (5-29%)
Nicolaides-Baraitser syndrome
Very frequent (80-99%)
Pitt-Hopkins syndrome
Very frequent (80-99%)
Spinocerebellar ataxia type 29
Always present (100%)
Citrullinemia type II
Occasional (5-29%)
Behavioral variant of frontotemporal dementia
Very frequent (80-99%)
15q11q13 microduplication syndrome
Always present (100%)
Filippi syndrome
Very frequent (80-99%)
Microphthalmia with linear skin defect syndrome
Occasional (5-29%)
Epidermolysis bullosa simplex with muscular dystrophy
Very frequent (80-99%)
Isodicentric chromosome 15 syndrome
Frequent (30-79%)
X-linked intellectual disability Hedera type
Occasional (5-29%)
X-linked intellectual disability Nascimento type
Frequent (30-79%)
17p11.2 microduplication syndrome
Very frequent (80-99%)
Helsmoortel-van der Aa syndrome
Occasional (5-29%)
Hypertrichosis cubiti
Frequent (30-79%)
Thumb deformity, alopecia, pigmentation anomaly syndrome
Frequent (30-79%)
Neuhauser Eichner Opitz syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 64712007
- UMLS CUI
- C0013528
- Fully Specified Name
- Echolalia (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.