Beckwith-Wiedemann syndrome (Congenital Malformation Syndromes))
1p36 deletion (monosomy) syndrome
Lumbar spondylolysis
S100 protein, CSF
Juvenile polyposis syndrome
X-Inactivation (XIST), Xq13.2 Deletion
Prolactinoma
Estriol, Unconjugated, Serum
Bacterial pneumonia
Henoch-Schönlein purpura
LDS
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Upper gastrointestinal hemorrhage
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Upper gastrointestinal hemorrhage
Disease
SNOMED
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Upper gastrointestinal hemorrhage
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