Page 199 - Standard Dental

1 SNODENT ID
4845 173317D
4846 112499D
141731D
4848 166967D
4849 144008D
4850 185660D
4851 142151D
4852 132149D
4853 141071D
4854 167407D
4855 144054D
4856 172231D
4857 105636D
4858 185401D
4859 107175D
4860 184814D
4861 184814D
4862
4863 169666D
4864 123576D
101389D
4866 175129D
4867 126380D
4868 129432D
4869 146862D
4870 142935D
4871 135339D
SNODENT TERM
Hemolysis (finding) Hemolytic anemia (disorder)
Hemolytic disease of fetus OR newborn due to isoimmunization
Hemolytic disorder
Hemolytic jaundice
Hemolytic uremic syndrome
Hemophilia (disorder)
Hemophilia - specialty (qualifier value)
Hemorrhage (morphologic abnormality)
Hemorrhagic cyst
Hemorrhagic cyst of jaw
Hemorrhagic inflammation (morphologic abnormality)
Hemorrhagic stomatitis
Hemorrhoids
Henck-Assman disease?
Henoch-Schönlein purpura?
Immunoglobulin A vasculitis (disorder)
Hepatitis C virus (organism)
Hereditary angioedema (disorder)
Hereditary benign intraepithelial dyskeratosis (disorder)
Hereditary disease
Hereditary factor IX deficiency disease
Hereditary factor VIII deficiency disease
Hereditary gingival fibromatosis Hereditary hemochromatosis
Hereditary motor neuron disease
SYNONYM ID
SYNONYM TERM
SD ID
DX173317 DX112499 DX141731
DX166967 DX144008 DX185660 DX142151 DX132149
DX141071
DX167407 DX144054 DX172231
DX105636 DX185401 DX107175 DX184814 DX184814
DX294344015 DX169666 DX123576
DX101389
DX175129 DX126380
DX129432
DX146862 DX142935 DX135339
SD TERM
Hemolysis (finding) Hemolytic anemia (disorder)
Hemolytic disease of fetus OR newborn due to isoimmunization
Hemolytic disorder
Hemolytic jaundice
Hemolytic uremic syndrome
Hemophilia (disorder)
Hemophilia - specialty (qualifier value)
Hemorrhage (morphologic abnormality)
Hemorrhagic cyst
Hemorrhagic cyst of jaw
Hemorrhagic inflammation (morphologic abnormality)
Hemorrhagic stomatitis
Hemorrhoids
Henck-Assman disease?
Henoch-Schönlein purpura?
Immunoglobulin A vasculitis (disorder)
Henoch-Schönlein purpura Hepatitis C virus (organism)
Hereditary angioedema (disorder)
Hereditary benign intraepithelial dyskeratosis (disorder)
Hereditary disease
Hereditary factor IX deficiency disease
Hereditary factor VIII deficiency disease
Hereditary gingival fibromatosis Hereditary hemochromatosis
Hereditary motor neuron disease
CDT ID
CDT TERMI
CD-10 TM IDI
CD-10 TM Term
4847
4865
294344015
Henoch-Schönlein purpura
STANDARD DENTAL
197
DATA SET