Overview
White forelock with malformations 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 palate morphology
Very frequent (80-99%)HP:0000174
Abnormality of the respiratory system
Very frequent (80-99%)HP:0002086
Atria septal defect
Very frequent (80-99%)HP:0001631
Curvature of little finger
Very frequent (80-99%)HP:0004209
Delayed skeletal development
Very frequent (80-99%)HP:0002750
Depressed philtrum
Very frequent (80-99%)HP:0002002
Grey sclerae
Very frequent (80-99%)HP:0000592
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Joint ligamentous laxity
Very frequent (80-99%)HP:0001382
Palpebronasal fold
Very frequent (80-99%)HP:0000286
Partial syndactyly
Very frequent (80-99%)HP:0006101
Poliosis of anterior hair
Very frequent (80-99%)HP:0002211
Posteriorly angulated ears
Very frequent (80-99%)HP:0000358
Turridolichocephaly
Very frequent (80-99%)HP:0000268
Near sighted
Frequent (30-79%)HP:0000545
Rib anomalies
Frequent (30-79%)HP:0000772
Spina bifida occulta
Frequent (30-79%)HP:0003298
Sprengel deformity
Frequent (30-79%)HP:0000912
Squint
Frequent (30-79%)HP:0000486
Bronchomalacia
HP:0002780
Hypoplasia/agenesis of distal phalanges of toes
HP:0010185
Patch of white hair
HP:0002290
Prominent veins on trunk
HP:0007457
Related Conditions
Congenital anomaly of skeletal bone(parent)
Congenital anomaly of cardiovascular system(parent)
Poliosis(parent)
Congenital anomaly of eye(parent)
Congenital anomaly of hair(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Cardiovascular system hereditary disorder(parent)
Hereditary disorder of the integument(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary disorder of the visual system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 763619009
- UMLS CUI
- C1848463
- Fully Specified Name
- White forelock with malformations syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.