| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0004368 |
BXGD000271 |
Autoimmune state |
|
| C0011168 |
BXGD000700 |
Deglutition Disorders |
Digestive System Diseases; Otorhinolaryngologic Diseases |
| C0017168 |
BXGD001101 |
Gastroesophageal reflux disease |
Digestive System Diseases |
| C0022680 |
BXGD001576 |
Polycystic Kidney Diseases |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023186 |
BXGD001613 |
Learning Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0026837 |
BXGD001937 |
Muscle Rigidity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0027498 |
BXGD001994 |
Nausea and vomiting |
Pathological Conditions, Signs and Symptoms |
| C0034069 |
BXGD002458 |
Pulmonary Fibrosis |
Respiratory Tract Diseases |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0037299 |
BXGD002685 |
Skin Ulcer |
Skin and Connective Tissue Diseases |
| C0158113 |
BXGD003875 |
Contracture of joint of hand |
Musculoskeletal Diseases |
| C0206138 |
BXGD004158 |
CREST Syndrome |
Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Cardiovascular Diseases |
| C0343149 |
BXGD007606 |
Contracture of joint of foot |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0424790 |
BXGD008543 |
Rigor - Temperature-associated observation |
Pathological Conditions, Signs and Symptoms |
| C0476254 |
BXGD008984 |
Dyslexia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0748540 |
BXGD010199 |
Scleroderma, Limited |
Skin and Connective Tissue Diseases |
| C0871215 |
BXGD011313 |
Reading Disabilities |
|
| C0920296 |
BXGD011464 |
Developmental reading disorder |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C1836735 |
BXGD014155 |
hypopigmented skin patch |
Skin and Connective Tissue Diseases |
| C1837249 |
BXGD014210 |
Malformations of Cortical Development, Group II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1868720 |
BXGD016531 |
Periventricular Nodular Heterotopia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C2973725 |
BXGD018205 |
Pulmonary arterial hypertension |
Respiratory Tract Diseases; Cardiovascular Diseases |
| C3203102 |
BXGD018555 |
Idiopathic pulmonary arterial hypertension |
Respiratory Tract Diseases |
| C4021910 |
BXGD020836 |
Narrow foramen obturatorium |
|
| C4022018 |
BXGD020872 |
Telangiectasia of the skin |
Cardiovascular Diseases |
| C4022020 |
BXGD020873 |
Mucosal telangiectasiae |
Cardiovascular Diseases |
| C4552000 |
BXGD023473 |
Episodic Kinesigenic Dyskinesia 1 |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |