| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0002884 |
BXGD000143 |
Hypochromic anemia |
Hemic and Lymphatic Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0015300 |
BXGD000973 |
Exophthalmos |
Eye Diseases |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0016049 |
BXGD001039 |
Fibromatosis, Gingival |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0017565 |
BXGD001118 |
Gingival Hemorrhage |
Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0018777 |
BXGD001217 |
Conductive hearing loss |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0018784 |
BXGD001220 |
Sensorineural Hearing Loss (disorder) |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0151849 |
BXGD003486 |
Alkaline phosphatase raised |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0158570 |
BXGD003892 |
Vascular anomaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0221766 |
BXGD004478 |
Diastasis recti |
Musculoskeletal Diseases; Wounds and Injuries |
| C0239174 |
BXGD004969 |
Late tooth eruption |
|
| C0278878 |
BXGD006609 |
Adult Glioblastoma |
Neoplasms |
| C0280474 |
BXGD006748 |
Childhood Glioblastoma |
Neoplasms |
| C0796133 |
BXGD010801 |
Ramon Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms |
| C0870082 |
BXGD011309 |
Hyperkeratosis |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1306503 |
BXGD012363 |
Congenital exomphalos |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1306710 |
BXGD012372 |
Facial asymmetry |
Pathological Conditions, Signs and Symptoms |
| C1314665 |
BXGD012386 |
Serum alkaline phosphatase raised |
|
| C1398312 |
BXGD012999 |
Narrow palate |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1847197 |
BXGD014856 |
Vascular Malformation, Primary Intraosseous |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C1849211 |
BXGD015023 |
Generalized hirsutism |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1862475 |
BXGD016132 |
Abnormality of retinal pigmentation |
|
| C1866231 |
BXGD016388 |
Full cheeks |
|
| C1961121 |
BXGD016675 |
Congenital vascular anomaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C3152182 |
BXGD018461 |
Anterior chamber anomalies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3665346 |
BXGD019278 |
Unspecified visual loss |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C3665347 |
BXGD019279 |
Visual Impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3665386 |
BXGD019284 |
Abnormal vision |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C4021800 |
BXGD020790 |
Abnormality of dental enamel |
|
| C4022018 |
BXGD020872 |
Telangiectasia of the skin |
Cardiovascular Diseases |
| C4539078 |
BXGD023225 |
Supraumbilical raphe |
|
| C4553962 |
BXGD023553 |
Hyperkeratosis, CTCAE |
|
| C4721411 |
BXGD023735 |
Osteolysis |
Musculoskeletal Diseases |