Overview
Czeizel Losonci 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.
Abnormality of the urinary system
Frequent (30-79%)HP:0000079
Foot ectrodactyly
Frequent (30-79%)HP:0001839
Hydronephrosis
Frequent (30-79%)HP:0000126
Lobster claw hand
Frequent (30-79%)HP:0100257
Posterolateral diaphragmatic hernia
Frequent (30-79%)HP:0025193
Split spine
Frequent (30-79%)HP:0002414
Ureteral agenesis
Frequent (30-79%)HP:0012300
2-3 finger cutaneous syndactyly
Occasional (5-29%)HP:0001233
Abnormality of the mediastinum
Occasional (5-29%)HP:0045026
Clubbing of toes
Occasional (5-29%)HP:0100760
Congenital megaureter
Occasional (5-29%)HP:0008676
Heart tip and four chambers point towards right side of body
Occasional (5-29%)HP:0001651
High arched palate
Occasional (5-29%)HP:0000218
Hitchhiker thumb
Occasional (5-29%)HP:0001234
Hypoplastic helices
Occasional (5-29%)HP:0008589
Hypoplastic mandible
Occasional (5-29%)HP:0000347
Hypoplastic nipples
Occasional (5-29%)HP:0002557
Left diaphragmatic hernia
Occasional (5-29%)HP:0009112
Mongoloid slant
Occasional (5-29%)HP:0000582
Myelomeningocele
Occasional (5-29%)HP:0002475
Nonsyndromal hydrocephalus
Occasional (5-29%)HP:0000238
Poorly developed lungs
Occasional (5-29%)HP:0002089
Posteriorly angulated ears
Occasional (5-29%)HP:0000358
Prominent antitragus
Occasional (5-29%)HP:0008593
Single flexion crease
Occasional (5-29%)HP:0000954
Sloping forehead
Occasional (5-29%)HP:0000340
Spina bifida occulta
Occasional (5-29%)HP:0003298
Thickened skin folds of neck
Occasional (5-29%)HP:0000474
Thin skull bone
Occasional (5-29%)HP:0010539
Thoracolumbar scoliosis
Occasional (5-29%)HP:0002944
Related Conditions
Autosomal dominant hereditary disorder(parent)
Congenital cleft hand(parent)
Multiple malformation syndrome with limb defect as major feature(parent)
Spina bifida(parent)
Congenital malformation of the urinary system(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary disorder of nervous system(parent)
Hereditary disorder of the urinary system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 732927000
- UMLS CUI
- C1866739
- Fully Specified Name
- Split hand, obstructive uropathy, spina bifida, diaphragmatic defect 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.