Condition

Butterfly Rash

phenotype

phenotype · Skin and Connective Tissue Diseases

Butterfly Vertebrae

phenotype

phenotype

Butterfly Vertebral Arch

phenotype

phenotype

Butterfly-Shaped Pigmentary Macular Dystrophy

syndrome

disease

Butyrylcholinesterase Deficiency

syndrome

disease · Respiratory Tract Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms

Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Byssinosis

syndrome

ICD-10 J66.0

disease · Occupational Diseases; Respiratory Tract Diseases

Byzanthine Arch Palate

disease

disease · Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases

C Cell Tumor

disease

disease · Neoplasms

C-Cell Hyperplasia of Thyroid

syndrome

disease · Endocrine System Diseases; Pathological Conditions, Signs and Symptoms

C-Reactive Protein Measurement

phenotype

phenotype

C1-C2 Subluxation

phenotype

phenotype

C1-C2 Vertebral Abnormality

disease

disease

C1Q Deficiency

syndrome

disease

C2-C3 Subluxation

phenotype

phenotype

C3 Glomerulonephritis

syndrome

disease · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications

C3 Glomerulopathy

syndrome

disease

C3Hex, Ability To Smell

phenotype

phenotype

C4 Complement Assay (Procedure)

phenotype

phenotype

C4 Deficiency

syndrome

disease

C5 Palsy

syndrome

disease

C7 And C6 Deficiency, Combined Subtotal

disease

disease

C8 Deficiency

phenotype

phenotype

C9 Deficiency

syndrome

disease · Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Cachexia

phenotype

ICD-10 R64

phenotype · Pathological Conditions, Signs and Symptoms

Cacosmia

syndrome

disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cadasil Syndrome

syndrome

disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cadasilm

syndrome

disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Cadmium Poisoning

disease

disease · Chemically-Induced Disorders

Cafe Au Lait Spots, Multiple

syndrome

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Cafe-Au-Lait Macules With Pulmonary Stenosis

syndrome

disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms

Cafe-Au-Lait Spots

phenotype

ICD-10 L81.3

phenotype · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Caffeine Dependence

phenotype

phenotype · Mental Disorders; Chemically-Induced Disorders

Caffeine Related Disorders

group

group

Caffeine Withdrawal

disease

disease

Cakut

syndrome

disease · Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications

Calcaneal Apophysitis

syndrome

disease · Skin and Connective Tissue Diseases; Musculoskeletal Diseases

Calcaneal Epiphyseal Stippling

phenotype

phenotype

Calcaneonavicular Fusion

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases

Calcaneovalgus Deformity

disease

disease

Calcific Stenosis

disease

disease · Pathological Conditions, Signs and Symptoms

Calcific Stippling

phenotype

phenotype

Calcific Stippling of Infantile Cartilaginous Skeleton

phenotype

phenotype

Calcific Tendinitis

syndrome

ICD-10 M65.2

disease · Wounds and Injuries; Musculoskeletal Diseases

Calcification of Cartilage

phenotype

phenotype

Calcification of Coronary Artery

phenotype

phenotype · Cardiovascular Diseases; Nutritional and Metabolic Diseases

Calcification of Falx Cerebri

syndrome

disease

Calcification of Joints And Arteries

syndrome

disease · Cardiovascular Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases