Overview
Verheij syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cleft of palate
Always present (100%)HP:0000175
Decreased size of cranium
Always present (100%)HP:0000252
Growth deficiency
Always present (100%)HP:0001510
Hemivertebra
Always present (100%)HP:0002937
Retrognathia
Always present (100%)HP:0000278
Decreased body height
Very frequent (80-99%)HP:0004322
Mental and motor retardation
Very frequent (80-99%)HP:0001263
Moderate mental retardation
Very frequent (80-99%)HP:0002342
Abnormal hands
Frequent (30-79%)HP:0001155
Asymmetric ears
Frequent (30-79%)HP:0010722
Autism spectrum disorder
Frequent (30-79%)HP:0000729
Big cheeks
Frequent (30-79%)HP:0000293
Bilateral fifth digit clinodactyly
Frequent (30-79%)HP:0004209
Broad, upturned nose
Frequent (30-79%)HP:0000455
Cardiac anomaly
Frequent (30-79%)HP:0001627
Curvature of finger
Frequent (30-79%)HP:0040019
Decreased visual acuity
Frequent (30-79%)HP:0007663
Decreased volume of upper lip
Frequent (30-79%)HP:0000219
Expressive language delay
Frequent (30-79%)HP:0002474
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
Flat philtrum
Frequent (30-79%)HP:0000319
Increased length of philtrum
Frequent (30-79%)HP:0000343
Increased width of bridge of nose
Frequent (30-79%)HP:0000431
Joint ligamentous laxity
Frequent (30-79%)HP:0001382
Nasogastric tube feeding in infancy
Frequent (30-79%)HP:0011470
Nostrils anteverted
Frequent (30-79%)HP:0000463
Palpebronasal fold
Frequent (30-79%)HP:0000286
Pes valgus
Frequent (30-79%)HP:0008081
Posteriorly angulated ears
Frequent (30-79%)HP:0000358
Short neck
Frequent (30-79%)HP:0000470
Related Conditions
Autosomal dominant hereditary disorder(parent)
Developmental delay(parent)
8q partial monosomy syndrome(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Congenital anomaly of musculoskeletal system(parent)
Genetic intellectual disability(parent)
Abnormality of skeleton morphology(parent)
Quick Facts
- SNOMED CT
- 1229895008
- UMLS CUI
- C3810023
- Fully Specified Name
- 8q24.3 microdeletion syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.