Overview
Catel Manzke 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.
Pierre-Robin sequence
Always present (100%)HP:0000201
Anomaly of the epiphyses
Very frequent (80-99%)HP:0005930
Bilateral fifth digit clinodactyly
Very frequent (80-99%)HP:0004209
Cleft of palate
Very frequent (80-99%)HP:0000175
Hypoplastic mandible condyle
Very frequent (80-99%)HP:0000347
Hypotrophic malar bone
Very frequent (80-99%)HP:0000272
Undergrowth
Very frequent (80-99%)HP:0001508
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Chronic ear infection
Frequent (30-79%)HP:0000389
Chubby cheeks
Frequent (30-79%)HP:0000293
Cobb angle greater than ten degrees
Frequent (30-79%)HP:0002650
Decreased body height
Frequent (30-79%)HP:0004322
Growth delay as children
Frequent (30-79%)HP:0008897
Low-set ears
Frequent (30-79%)HP:0000369
Posteriorly angulated ears
Frequent (30-79%)HP:0000358
Stiff joint
Frequent (30-79%)HP:0001387
Thick, flared eyebrows
Frequent (30-79%)HP:0002553
Thin eyebrow
Frequent (30-79%)HP:0045074
VSD
Frequent (30-79%)HP:0001629
Atria septal defect
Occasional (5-29%)HP:0001631
Collapsed nostrils
Occasional (5-29%)HP:0009933
Columella, low insertion
Occasional (5-29%)HP:0010763
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
Genu valga
Occasional (5-29%)HP:0002857
High arched palate
Occasional (5-29%)HP:0000218
Humeral hypoplasia
Occasional (5-29%)HP:0005792
Increased distance between eyes
Occasional (5-29%)HP:0000316
Lacrimal duct obstruction
Occasional (5-29%)HP:0000579
Ligamentous laxity
Occasional (5-29%)HP:0001382
Metatarsus valgus
Occasional (5-29%)HP:0010508
Related Conditions
Congenital anomaly of finger(parent)
Multiple malformation syndrome with limb defect as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Dysostosis(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Abnormality of index finger morphology(parent)
Quick Facts
- SNOMED CT
- 722383001
- UMLS CUI
- C1844887
- Fully Specified Name
- Catel Manzke 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.