Body system structure
Organ system
Body system structure (body structure)
91689009
http://purl.bioontology.org/ontology/SNOMEDCT/91689009
0
Xa1gC
Manual rotation of fetal head
Drop arm test
Adductor pollicis test
Internal cephalic version and extraction
Abbott-Saunders test
Stress test - finger metacarpophalangeal collateral ligament
Stress test of finger collateral ligament
Tennis elbow test
Suprapubic pressure on fetal shoulder
Upper limb tension test with median nerve bias
Stress test - finger proximal interphalangeal collateral ligament
Wood's screw maneuver
Examination of joint movement
Allen's test
Dix-Hallpike maneuver
Stress test - finger distal interphalangeal collateral ligament
Modified Schober test
Upper limb tension test with ulnar nerve bias
Bowstring test
Ultrasound procedure on endocrine system
Yergason's test
Freeing the posterior arm
Ultrasound procedure on nervous system AND/OR special sense organ
Examination of muscle power
Schamroth test
Examination of pain sensation
Bracht maneuver
Shoulder maneuver
Intrinsic-plus test
Elbow maneuver
Examination of pulse
Elbow flexion test
Reverse intrinsic-plus test
Fajersztajn test
Ultrasound studies of systems
Wrist maneuver
Hand maneuver
Sitting root test
Replacement of prolapsed umbilical cord
Modified Adson's test
Physical examination maneuver related to cervical spine
Stress test of hand collateral ligament
Milgram test
Manual procedure for malpresentation or position
Internal conversion of face to vertex
Examination of blood pressure
Examination of gait
Costoclavicular maneuver
Maneuvers for delivery in shoulder dystocia
Head distraction test
Reposition of a prolapsed arm
Upper limb tension test
Queckenstedt's test
Haagensen test
Physical examination maneuver related to thoracic outlet
Physical examination maneuver related to upper extremity
Face to pubes conversion
Flexion test
McRoberts maneuver
Erichsen's test
Obstetrics manipulation
Chin to chest distance
Physical examination maneuver
General appraisal of hearing
Fluoroscopy and radiography - digestive
Upper limb tension test with radial nerve bias
Examination of body system
Crossed straight leg test
Wigand-Martin maneuver
Pinard maneuver
Examination of body function
Prague maneuver
Delivery by Ritgen maneuver
Fetal head - manual flexion
Fluoroscopy of systems
Digestive system fluoroscopy
Iliac compression test
Adson's test
Spurling maneuver
Gaenslen's test
Wigand's obstetrical version
Shoulder depression test
Paper-pulling test
Apprehension test
Manually assisted spontaneous delivery
CT of systems
Buerger's test
Physical examination maneuver related to pelvis
Ely's test
Physical examination maneuver related to the spine
Stress test of thumb collateral ligament
Van Hoorn maneuver
Stress test - thumb interphalangeal collateral ligament
Stress test - thumb metacarpophalangeal collateral ligament
Finger-to-floor distance test
Secondary bitter taste disorder
Hemoglobin S sickling disorder without crisis
Hemoglobin Lepore trait
Homozygous beta thalassemia
HNSHA due to phosphofructokinase deficiency
Hemoglobin SS disease without crisis
delta beta^0^ Thalassemia
Thalassemia
Hereditary elliptocytosis
Alpha trait thalassemia
Hereditary red blood cell disorder
delta beta Thalassemia
Hereditary spherocytosis
SCID due to absent class II HLA antigens
Sickle cell-hemoglobin D disease without crisis
Hereditary pyropoikilocytosis
HNSHA due to diphosphoglycerate mutase deficiency
Double heterozygous sickling disorder
Chronic granulomatous disease
Adenosine deaminase deficiency
Unstable hemoglobin disease
Homozygous alpha thalassemia
HNSHA due to aldolase A deficiency
alpha Thalassemia
Beta thalassemia trait
Hb SS disease
Sickle cell-hemoglobin E disease
Hereditary hemoglobinopathy due to globin chain mutation
Hereditary disorder by system
Connective tissue hereditary disorder
Complement component deficiency
SCID due to absent IL-2 production
alpha^0^ Thalassemia
Gamma thalassemia
Heterozygous thalassemia
Delta-beta-Lepore thalassemia
Chronic granulomatous disease, type III
Nezelof's syndrome
HNSHA due to pyrimidine-5'-nucleotidase deficiency
Chronic granulomatous disease, type I
Hereditary elliptocytosis due to alpha spectrin defect
Hereditary hypersegmentation
A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
Thalassemia with other hemoglobinopathy
Chronic granulomatous disease, type IA
X-linked severe combined immunodeficiency
SCID due to absent peripheral T cell maturation
Hereditary hemoglobin S
Hereditary hemoglobinopathy
Hereditary persistence of fetal hemoglobin
Hereditary white blood cell disorder
HNSHA due to pyruvate kinase deficiency
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
Primary acid taste disorder
Hereditary elliptocytosis due to abnormal protein 4.1
Hemoglobin H disease
Hemoglobin M disease
Sickle cell-hemoglobin D disease with crisis
epsilon gamma delta beta Thalassemia
HNSHA due to glutathione synthetase deficiency
Primary salt taste disorder
Hemoglobin H constant spring thalassemia
Hereditary disorder of immune system
beta Thalassemia
Hemoglobin C trait
HNSHA due to phosphoglycerate kinase deficiency
Secondary taste disorder
HNSHA due to NADH-methemoglobin reductase deficiency
Disorder of taste
HPFH unlinked to beta-globulin gene cluster
delta^0^ Thalassemia
Hemoglobin S sickling disorder with crisis
alpha^+^ Thalassemia
Alpha-beta thalassemia
Chagas' mega disease
Sickle cell trait with coexistent alpha-thalassemia
Sickle cell-hemoglobin E disease without crisis
Sickle cell-hemoglobin C disease with crisis
Hemoglobin SS disease with crisis
beta^+^ Thalassemia, normal Hb A>2
HPFH deletion type
Sickle cell trait
Beta thalassemia intermedia
Hereditary nonspherocytic hemolytic anemia
Hereditary persistence of fetal hemoglobin thalassemia
Congenital methemoglobinemia with abnormal methemoglobins
HPFH delta beta^0^ thalassemia
Hereditary elliptocytosis due to beta spectrin defect in self-association
Sequelae of disorders classified by disorder-system
Hemoglobin O-Arab trait
Secondary salt taste disorder
Severe combined immunodeficiency disease
Alpha thalassemia-2 trait
Hemoglobin D trait
HNSHA due to triosephosphate isomerase deficiency
Hemoglobin C disease
Anterior tongue taste disorder
X chromosome-linked pyridoxine refractory sideroblastic anemia
Hemolytic anemia due to pyruvate kinase deficiency
epsilon gamma delta beta^0^ Thalassemia
Homozygous hemoglobinopathy
HNSHA due to gamma glutamyl cysteine synthetase deficiency
Sickle cell-hemoglobin C disease
HPFH linked to beta-globulin gene cluster
HNSHA due to hexokinase deficiency
Thalassemia major
Acquired hemoglobin H disease
SCID due to absent adenosine deaminase
Chronic granulomatous disease, type IV
Hemoglobin E/beta thalassemia disease
Autosomal recessive SCID
SCID due to absent IL-2 receptor
Hereditary eosinophilia
Chronic granulomatous disease, type II
Hereditary sideroblastic anemia
Thalassemia intermedia
Sickle cell-hemoglobin E disease with crisis
Secondary acid taste disorder
HNSHA due to glucose phosphate isomerase deficiency
Heritable disorder of neutrophil production
HNSHA due to increased adenosine deaminase activity
Hemoglobin E disease
Sickle cell-hemoglobin Lepore disease
Hemoglobin D disease
Hereditary elliptocytosis with transient poikilocytosis
beta^0^ Thalassemia
Inflammation of specific body systems
Jung syndrome
HPFH nondeletion type
Hereditary elliptocytosis due to deficiency of protein 4.1
SCID due to absent lymphoid stem cells
Sickle cell-hemoglobin D disease
Secondary sweet taste disorder
Hereditary hemolytic anemia
Hemoglobin Constant Spring trait
Hemolytic anemia due to triose phosphate isomerase deficiency
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
SCID due to absent T cell receptor
HNSHA due to decreased adenosine deaminase activity
Heterozygous hemoglobinopathy
Sickling disorder due to hemoglobin S
Hemolytic anemia due to glutathione metabolism disorder
Chronic granulomatous disease, type IIA
X chromosome-linked pyridoxine responsive sideroblastic anemia
^A^gamma delta beta^0^ thalassemia
Chronic granulomatous disease, type IVA
HPFH A gamma beta^+^ thalassemia
beta^0^ Thalassemia, nondeletion type
Hemoglobin SS disease with vasoocclusive crisis
Hemoglobin Bart's hydrops syndrome
Hereditary disorder of cellular element of blood
Sickle cell-hemoglobin C disease without crisis
Thalassemia syndrome
Sickle cell-Hemoglobin O Arab disease
Primary bitter taste disorder
Hereditary elliptocytosis due to glycophorin C deficiency
HNSHA due to NADH diaphorase deficiency
Heritable disorder of neutrophil function
Hb Lepore thalassemia
alpha^+^ Thalassemia, deletion type
Alpha thalassemia-mental retardation syndrome
HNSHA due to glutathione reductase deficiency
Primary sweet taste disorder
Disorder of body system
beta^+^ Thalassemia
Siccardi syndrome
HPFH G gamma beta^+^ thalassemia
Primary taste disorder
beta^0^ Thalassemia, deletion type
Thalassemia-hemoglobin C disease
Autosomal recessive severe combined immunodeficiency
delta Thalassemia
Hemoglobin E trait
alpha^+^ Thalassemia, nondeletion type
Obstetric injection
Anatomical structure
1
Entire body as a whole
Blood/lymphatic operations
Nuclear medicine study of systems
Nuclear medicine diagnostic procedure on endocrine AND/OR hematopoietic system
Procedure on body system
Body system
Body System
T-D0046
T022
C0460002
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