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Marden Walker syndrome

disorder
SNOMED 449824004CUI C0796033

Overview

Marden Walker 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.

Dandy-Walker cyst
Always present (100%)HP:0001305
Absent/small skeletal muscles
Very frequent (80-99%)HP:0001460
Arachnodactyly
Very frequent (80-99%)HP:0001166
Arthrogryposis multiplex
Very frequent (80-99%)HP:0002804
Blepharophimosis
Very frequent (80-99%)HP:0000581
Cleft of palate
Very frequent (80-99%)HP:0000175
Cognitive delay
Very frequent (80-99%)HP:0001263
Decreased size of cranium
Very frequent (80-99%)HP:0000252
Eyelid ptosis
Very frequent (80-99%)HP:0000508
Feeding difficulties
Very frequent (80-99%)HP:0011968
Fused forearm bones
Very frequent (80-99%)HP:0002974
Hypoplastic mandible
Very frequent (80-99%)HP:0000347
Low-set ears
Very frequent (80-99%)HP:0000369
Mask-like facies
Very frequent (80-99%)HP:0000298
Mental deficiency
Very frequent (80-99%)HP:0001249
Muscle atrophy, neurogenic
Very frequent (80-99%)HP:0003202
Muscular dystrophy
Very frequent (80-99%)HP:0003560
Narrow mouth
Very frequent (80-99%)HP:0000160
Peripheral hypotonia
Very frequent (80-99%)HP:0001252
Poor growth
Very frequent (80-99%)HP:0001510
Posteriorly angulated ears
Very frequent (80-99%)HP:0000358
Retrognathia
Very frequent (80-99%)HP:0000278
Short palpebral fissure
Very frequent (80-99%)HP:0012745
Short stature, severe
Very frequent (80-99%)HP:0003510
Specific learning disability
Very frequent (80-99%)HP:0001328
Stiff joint
Very frequent (80-99%)HP:0001387
Submucous cleft hard palate
Very frequent (80-99%)HP:0000176
Undergrowth
Very frequent (80-99%)HP:0001508
Uvula bifida
Very frequent (80-99%)HP:0000193
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018

Related Conditions

Arthrogryposis multiplex congenita(parent)
Inherited arthrogryposis(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT
449824004
UMLS CUI
C0796033
Fully Specified Name
Marden Walker 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.