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Query OMIM entry list
176860
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PROTEIN C DEFICIENCY, CONGENITAL THROMBOTIC DISEASE DUE TO
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Body Regions
Extremities
Lower Extremity
Foot
Forefoot, Human
Toes
Musculoskeletal System
Skeleton
Bone and Bones
Bones of Lower Extremity
Leg Bones
Femur
Digestive System
Liver
Urogenital System
Urinary Tract
Kidney
Kidney Cortex
Kidney Glomerulus
Glomerular Filtration Barrier
Podocytes
Nephrons
Kidney Glomerulus
Podocytes
Cardiovascular System
Blood Vessels
Arteries
Endothelium, Vascular
Veins
Femoral Vein
Renal Veins
Tissues
Epithelium
Endothelium
Endothelium, Vascular
Exocrine Glands
Mammary Glands, Animal
Cells
Cells, Cultured
Cell Line
Cell Line, Transformed
Cell Line, Tumor
HeLa Cells
CHO Cells
Hybrid Cells
Tumor Cells, Cultured
Cell Line, Tumor
HeLa Cells
Cellular Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 3
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 9
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Intracellular Space
Cell Nucleus
Cytoplasm
Cytoplasmic Structures
Organelles
Cell Nucleus
Endoplasmic Reticulum
Endoplasmic Reticulum, Rough
Golgi Apparatus
Ribosomes
Polyribosomes
Endoplasmic Reticulum, Rough
Endocrine Cells
Trophoblasts
Epithelial Cells
CHO Cells
HeLa Cells
Podocytes
Fluids and Secretions
Bodily Secretions
Milk
Body Fluids
Blood
Fetal Blood
Plasma
Serum
Immune Sera
Extracellular Fluid
Plasma
Animal Structures
Mammary Glands, Animal
Hemic and Immune Systems
Blood
Fetal Blood
Plasma
Embryonic Structures
Embryo, Mammalian
Blastocyst
Trophoblasts
Fetus
Fetal Blood
Placenta
Trophoblasts
Integumentary System
Skin
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