Condition
30,467 condition in the knowledge graph · page 93.
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Blepharoptosis
syndrome
ICD-10 H02.4
disease · Eye Diseases
Blepharospasm
syndrome
ICD-10 G24.5
disease · Eye Diseases
Blepharospasm, Benign Essential, Susceptibility To
phenotype
phenotype
Blind Loop Syndrome
syndrome
disease · Digestive System Diseases; Nutritional and Metabolic Diseases
Blind Vagina
disease
disease
Blind-Spot Enlargment
phenotype
phenotype
Blindness
phenotype
phenotype · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness Both Eyes Nos (Disorder)
phenotype
ICD-10 H54.0
phenotype · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness of One Eye (Disorder)
syndrome
ICD-10 H54.4
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Acquired
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Cortical
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Hysterical
phenotype
phenotype · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Legal
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Monocular
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blindness, Transient
phenotype
phenotype · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Blister With Infection
syndrome
disease · Skin and Connective Tissue Diseases; Infections; Pathological Conditions, Signs and Symptoms
Bloch Sulzberger Syndrome
syndrome
ICD-10 Q82.3
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Block Vertebrae
phenotype
phenotype
Blomstrand Dysplasia
syndrome
disease
Blonde Hair
phenotype
phenotype
Blood Autoimmune Disorders
group
group · Immune System Diseases; Hemic and Lymphatic Diseases
Blood Basophil Count (Lab Test)
phenotype
phenotype
Blood Coagulation Disorders
group
ICD-10 D68.9
group · Hemic and Lymphatic Diseases
Blood Coagulation Disorders, Inherited
group
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Blood Gases Abnormal
phenotype
phenotype
Blood Group Antigen Abnormality
phenotype
phenotype
Blood Group Deletion Syndrome
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Blood Group Incompatibility
syndrome
disease
Blood Group--Froese
phenotype
phenotype
Blood Group--Lutheran Null
phenotype
phenotype
Blood Group--Waldner Type
phenotype
phenotype
Blood Group--Wright Antigen
phenotype
phenotype
Blood group, Yt system
disease
Blood In Stool
phenotype
phenotype · Digestive System Diseases; Pathological Conditions, Signs and Symptoms
Blood Phenylalanine Measurement By Guthrie Microbiologic Assay
phenotype
phenotype
Blood Platelet Disorders
group
group · Hemic and Lymphatic Diseases
Blood Pressure
phenotype
phenotype
Blood Pressure Disorders
group
group · Cardiovascular Diseases
Blood Protein Measurement
phenotype
phenotype
Blood Sedimentation
phenotype
phenotype
Blood Spots
syndrome
disease
Blood Thyroid Stimulating Hormone Analysis
phenotype
phenotype
Blood Type Incompatibility
syndrome
disease
Blood Urea Increased
phenotype
phenotype · Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Blood Urea Nitrogen Measurement
phenotype
phenotype
Blood Vessel Tumors
group
group · Neoplasms
Blood Viscosity
phenotype
phenotype
Bloom Syndrome
syndrome
disease · Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases