| C0002726 |
BXGD000125 |
Amyloidosis |
Nutritional and Metabolic Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0008626 |
BXGD000559 |
Congenital chromosomal disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0015625 |
BXGD001006 |
Fanconi Anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0017612 |
BXGD001129 |
Glaucoma, Open-Angle |
Eye Diseases |
| C0019693 |
BXGD001346 |
HIV Infections |
Infections; Immune System Diseases |
| C0028840 |
BXGD002089 |
Ocular Hypertension |
Eye Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0152025 |
BXGD003521 |
Polyneuropathy |
Nervous System Diseases |
| C0184567 |
BXGD004039 |
Acute onset pain |
Pathological Conditions, Signs and Symptoms |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0259749 |
BXGD005216 |
Autonomic neuropathy |
Nervous System Diseases |
| C0268407 |
BXGD005936 |
Senile cardiac amyloidosis |
Nutritional and Metabolic Diseases; Cardiovascular Diseases |
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0595921 |
BXGD009626 |
Intraocular pressure disorder |
Eye Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C1148551 |
BXGD011766 |
X-Linked Dyskeratosis Congenita |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases |
| C1504336 |
BXGD013137 |
Polypoidal choroidal vasculopathy |
|
| C1846142 |
BXGD014785 |
HOYERAAL-HREIDARSSON SYNDROME |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Hemic and Lymphatic Diseases; Behavior and Behavior Mechanisms |
| C2751492 |
BXGD017718 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C3469521 |
BXGD018910 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |