| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001623 |
BXGD000066 |
Adrenal gland hypofunction |
Endocrine System Diseases |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0022116 |
BXGD001531 |
Ischemia |
Pathological Conditions, Signs and Symptoms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025267 |
BXGD001845 |
Multiple Endocrine Neoplasia Type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0029443 |
BXGD002152 |
Osteomyelitis |
Infections; Musculoskeletal Diseases |
| C0175754 |
BXGD004015 |
Agenesis of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0206686 |
BXGD004241 |
Adrenocortical carcinoma |
Neoplasms; Endocrine System Diseases |
| C0282160 |
BXGD006797 |
Aplasia Cutis Congenita |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0405580 |
BXGD008325 |
Adrenal cortical hypofunction |
Endocrine System Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0848558 |
BXGD010882 |
Hypospadias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0919267 |
BXGD011426 |
ovarian neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0949595 |
BXGD011580 |
Gonadal Dysgenesis, 46,XX |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C1691215 |
BXGD013491 |
Penile hypospadias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2751824 |
BXGD017742 |
46, XY Disorders of Sex Development |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |