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Radioulnar synostosis with microcephaly and scoliosis syndrome

disorder
SNOMED 719162001CUI C3150890

Overview

Radioulnar synostosis with microcephaly and scoliosis 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.

Abnormal dermatoglyphics
Very frequent (80-99%)HP:0007477
Abnormality of the elbow
Very frequent (80-99%)HP:0009811
Abnormality of the philtrum
Very frequent (80-99%)HP:0000288
Curvature of little finger
Very frequent (80-99%)HP:0004209
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased size of cranium
Very frequent (80-99%)HP:0000252
Fused forearm bones
Very frequent (80-99%)HP:0002974
Mental and motor retardation
Very frequent (80-99%)HP:0001263
Mental-retardation
Very frequent (80-99%)HP:0001249
Palpebronasal fold
Very frequent (80-99%)HP:0000286
Partial syndactyly
Very frequent (80-99%)HP:0006101
Pectus carinatum
Very frequent (80-99%)HP:0000768
Premature birth
Very frequent (80-99%)HP:0001622
Retarded ossification
Very frequent (80-99%)HP:0002750
Rib anomalies
Very frequent (80-99%)HP:0000772
Scoliosis
Very frequent (80-99%)HP:0002650
Thick eyebrow
Very frequent (80-99%)HP:0000574
Tooth abnormalities
Very frequent (80-99%)HP:0000164
Unibrow
Very frequent (80-99%)HP:0000664

Quick Facts

SNOMED CT
719162001
UMLS CUI
C3150890
Fully Specified Name
Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
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.