| C0001080 |
BXGD000022 |
Achondroplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0005684 |
BXGD000319 |
Malignant neoplasm of urinary bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005695 |
BXGD000323 |
Bladder Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007124 |
BXGD000437 |
Noninfiltrating Intraductal Carcinoma |
Neoplasms |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0007302 |
BXGD000460 |
Cartilage Diseases |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0010278 |
BXGD000660 |
Craniosynostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0020437 |
BXGD001381 |
Hypercalcemia |
Nutritional and Metabolic Diseases |
| C0022548 |
BXGD001551 |
Keloid |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025990 |
BXGD001884 |
Micrognathism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0026707 |
BXGD001922 |
Mucopolysaccharidosis IV |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0027092 |
BXGD001971 |
Myopia |
Eye Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029410 |
BXGD002138 |
Osteoarthritis of hip |
Musculoskeletal Diseases |
| C0029422 |
BXGD002142 |
Osteochondrodysplasias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0152013 |
BXGD003516 |
Adenocarcinoma of lung (disorder) |
Neoplasms |
| C0153381 |
BXGD003626 |
Malignant neoplasm of mouth |
Neoplasms; Stomatognathic Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0220641 |
BXGD004305 |
Lip and Oral Cavity Carcinoma |
Neoplasms; Stomatognathic Diseases |
| C0221354 |
BXGD004446 |
Frontal bossing |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221357 |
BXGD004449 |
Brachydactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0231712 |
BXGD004519 |
Waddling gait |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0239138 |
BXGD004966 |
Hip joint varus deformity - observation |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0239399 |
BXGD004981 |
Short extremities |
|
| C0242383 |
BXGD005160 |
Age related macular degeneration |
Eye Diseases |
| C0265289 |
BXGD005502 |
Metaphyseal chondrodysplasia Schmid type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0265290 |
BXGD005503 |
Metaphyseal chondrodysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0265294 |
BXGD005506 |
Pyle metaphyseal dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0278601 |
BXGD006547 |
Inflammatory Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0343284 |
BXGD007613 |
Chondrodysplasia |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0410528 |
BXGD008430 |
Skeletal dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0410538 |
BXGD008434 |
Pseudoachondroplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0410606 |
BXGD008437 |
Cervical Disc Degenerative Disorder |
Musculoskeletal Diseases |
| C0432211 |
BXGD008737 |
Spondyloepimetaphyseal disorder |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0432215 |
BXGD008739 |
Progressive pseudorheumatoid dysplasia |
Musculoskeletal Diseases |
| C0544755 |
BXGD009310 |
Genu varum |
Musculoskeletal Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699885 |
BXGD009869 |
Carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0700635 |
BXGD009897 |
Strudwick syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0878659 |
BXGD011380 |
Disproportionate short stature |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1636149 |
BXGD013482 |
Macular dystrophy, corneal type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1658953 |
BXGD013486 |
tumor vasculature |
|
| C1834975 |
BXGD014004 |
Irregular acetabular roof |
|
| C1834980 |
BXGD014005 |
Metaphyseal cupping of proximal phalanges |
|
| C1835473 |
BXGD014033 |
Diaphyseal thickening |
|
| C1839829 |
BXGD014413 |
Short distal phalanx of finger |
|
| C1842153 |
BXGD014499 |
Irregular vertebral endplates |
|
| C1844704 |
BXGD014665 |
Platyspondyly |
|
| C1846950 |
BXGD014848 |
Short middle phalanx of finger |
|
| C1855171 |
BXGD015466 |
Metaphyseal cupping of metacarpals |
|
| C1859461 |
BXGD015895 |
Femoral bowing |
Musculoskeletal Diseases |
| C1859697 |
BXGD015922 |
Enlargement of the proximal femoral epiphysis |
|
| C1861519 |
BXGD016056 |
Moderately short stature |
|
| C2745963 |
BXGD017571 |
Kashin-Beck Disease |
Musculoskeletal Diseases |
| C2748503 |
BXGD017591 |
Corneal Dystrophy, Subepithelial Mucinous |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C3150077 |
BXGD018291 |
Mild short stature |
|
| C4021383 |
BXGD020620 |
Broad middle phalanx of finger |
|
| C4021598 |
BXGD020692 |
Distal tibial bowing |
|
| C4021611 |
BXGD020697 |
Abnormality of epiphysis morphology |
|
| C4021657 |
BXGD020724 |
Abnormality of bone mineral density |
|
| C4025047 |
BXGD021534 |
Proximal femoral metaphyseal abnormality |
|
| C4025814 |
BXGD021806 |
Abnormality of the metaphysis |
|
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|