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Morquio syndrome

disorder
SNOMED 378007CUI C0026707

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Treatments & Interventions

Elosulfase alfa

substance

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal metaphysis morphology
Very frequent (80-99%)HP:0000944
Anomaly of the epiphyses
Very frequent (80-99%)HP:0005930
Bowed long bones
Very frequent (80-99%)HP:0006487
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased bone mineral density Z score
Very frequent (80-99%)HP:0004349
Delayed skeletal development
Very frequent (80-99%)HP:0002750
Dental problems
Very frequent (80-99%)HP:0000164
Gait disturbance
Very frequent (80-99%)HP:0001288
Genu valga
Very frequent (80-99%)HP:0002857
Hypoacusis
Very frequent (80-99%)HP:0000365
Loose-jointedness
Very frequent (80-99%)HP:0001382
Mucopolysacchariduria
Very frequent (80-99%)HP:0008155
Pectus carinatum
Very frequent (80-99%)HP:0000768
Rib anomalies
Very frequent (80-99%)HP:0000772
Scarring or clouding of the cornea of the eye
Very frequent (80-99%)HP:0007957
Short neck
Very frequent (80-99%)HP:0000470
Shorter than typical length between neck and abdomen
Very frequent (80-99%)HP:0010306
Cobb angle greater than ten degrees
Frequent (30-79%)HP:0002650
Dental cavities
Frequent (30-79%)HP:0000670
Dystrophic tooth enamel
Frequent (30-79%)HP:0000682
Flattened vertebral bodies
Frequent (30-79%)HP:0000926
Greyish enamel
Frequent (30-79%)HP:0000683
Hernia
Frequent (30-79%)HP:0100790
Hunched back
Frequent (30-79%)HP:0002808
Joint dislocation
Frequent (30-79%)HP:0001373
Large mouth
Frequent (30-79%)HP:0000154
Nostrils anteverted
Frequent (30-79%)HP:0000463
Prominent swayback
Frequent (30-79%)HP:0003307
Spinal stenosis
Frequent (30-79%)HP:0003416
Thickened facial skin with coarse facial features
Frequent (30-79%)HP:0000280

Related Conditions

Mucopolysaccharidosis, MPS-IV-B(child)
Mucopolysaccharidosis, MPS-IV-A(child)
Mucopolysaccharidosis(parent)
Metabolic bone disease(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital osteodystrophy(parent)

Quick Facts

SNOMED CT
378007
UMLS CUI
C0026707
Fully Specified Name
Morquio syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Known Treatments
1
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.