Overview
Karsch Neugebauer 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.
Congenital nystagmus
HP:0006934
Foot ectrodactyly
HP:0001839
Hand monodactyly
HP:0004058
Involuntary, rapid, rhythmic eye movements
HP:0000639
Lens opacities
HP:0000518
Noninflammatory retina disease
HP:0000488
Split hand
HP:0001171
Squint
HP:0000486
Related Conditions
Autosomal dominant hereditary disorder(parent)
Congenital abnormality of hand and digits(parent)
Multiple malformation syndrome with limb defect as major feature(parent)
Dysostosis(parent)
Congenital anomaly of visual system(parent)
Split foot(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary disorder of the visual system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 722032005
- UMLS CUI
- C1866740
- Fully Specified Name
- Karsch Neugebauer syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.