AlternativeMed

Condition

30,467 condition in the knowledge graph · page 11.

Abnormal Visual Accommodation
phenotype
phenotype
Abnormal Visual Evoked Potential
phenotype
phenotype · Nervous System Diseases
Abnormal Visual Field Test
phenotype
phenotype
Abnormal Visual Fixation
phenotype
phenotype
Abnormal Vitamin B12 Level
phenotype
phenotype
Abnormal Vitreous Humor Morphology
disease
disease
Abnormal Vocal Cord Morphology
phenotype
phenotype
Abnormal Yolk Sac
disease
disease
Abnormalities of Placenta Or Umbilical Cord
disease
disease
Abnormalities, Drug-Induced
group
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Abnormality Iris Morphology
disease
disease
Abnormality of Abdomen Morphology
disease
disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Abnormality of Acetylcarnitine Metabolism
phenotype
phenotype
Abnormality of Alkaline Phosphatase Activity
phenotype
phenotype
Abnormality of Amino Acid Metabolism
phenotype
phenotype
Abnormality of Aortic Arch
disease
disease
Abnormality of Aortic Valve
disease
disease
Abnormality of B Cell Physiology
phenotype
phenotype
Abnormality of Bladder Morphology
phenotype
phenotype
Abnormality of Blood And Blood-Forming Tissues
disease
disease
Abnormality of Body Height
disease
disease
Abnormality of Bone Marrow Cell Morphology
disease
disease
Abnormality of Bone Marrow Stromal Cells
phenotype
phenotype
Abnormality of Bone Mineral Density
disease
disease
Abnormality of Brain Morphology
phenotype
phenotype
Abnormality of Brainstem Morphology
phenotype
phenotype
Abnormality of Buccal Mucosa
phenotype
phenotype
Abnormality of Calvarial Morphology
phenotype
phenotype
Abnormality of Canine
disease
disease
Abnormality of Carbohydrate Metabolism/Homeostasis
phenotype
phenotype
Abnormality of Cardiovascular System Morphology
disease
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Abnormality of Cellular Immune System
phenotype
phenotype
Abnormality of Central Motor Conduction
phenotype
phenotype
Abnormality of Central Sensory Function
phenotype
phenotype
Abnormality of Central Somatosensory Evoked Potentials
phenotype
phenotype
Abnormality of Chorioretinal Pigmentation
phenotype
phenotype
Abnormality of Chromosome Segregation
phenotype
phenotype
Abnormality of Chromosome Stability
phenotype
phenotype
Abnormality of Circulating Adrenocorticotropin Level
phenotype
phenotype
Abnormality of Circulating Cortisol Level
phenotype
phenotype
Abnormality of Circulating Enzyme Level
phenotype
phenotype
Abnormality of Circulating Leptin Level
phenotype
phenotype
Abnormality of Coagulation
phenotype
phenotype
Abnormality of Complement System
phenotype
phenotype
Abnormality of Connective Tissue
disease
disease
Abnormality of Coordination
phenotype
phenotype
Abnormality of Copper Homeostasis
phenotype
phenotype
Abnormality of Corneal Stroma
disease
disease
Page 11 of 635 · 30,467 total