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
Cleft of palate
Very frequent (80-99%)HP:0000175
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Hypotrophic malar bone
Very frequent (80-99%)HP:0000272
Permanent curving of the pinkie finger
Very frequent (80-99%)HP:0004209
Poor weight gain
Very frequent (80-99%)HP:0001508
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Chronic middle ear infection
Frequent (30-79%)HP:0000389
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
Hyperplasia of cheeks
Frequent (30-79%)HP:0000293
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
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
Joint ligamentous laxity
Occasional (5-29%)HP:0001382
Metatarsus valgus
Occasional (5-29%)HP:0010508
Mongoloid slant
Occasional (5-29%)HP:0000582
Narrow mouth
Occasional (5-29%)HP:0000160
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.