| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0002622 |
BXGD000119 |
Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0003090 |
BXGD000175 |
Ankylosis |
Musculoskeletal Diseases |
| C0003578 |
BXGD000211 |
Apnea |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0005745 |
BXGD000331 |
Blepharoptosis |
Eye Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0008925 |
BXGD000575 |
Cleft Palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0009319 |
BXGD000596 |
Colitis |
Digestive System Diseases |
| C0009375 |
BXGD000602 |
Colonic Neoplasms |
Digestive System Diseases; Neoplasms |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0024636 |
BXGD001793 |
Malocclusion |
Stomatognathic Diseases |
| C0025988 |
BXGD001883 |
Microglossia |
Stomatognathic Diseases |
| C0025990 |
BXGD001884 |
Micrognathism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0026034 |
BXGD001887 |
Microstomia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0033377 |
BXGD002406 |
Ptosis |
Pathological Conditions, Signs and Symptoms |
| C0035126 |
BXGD002509 |
Reperfusion Injury |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0037384 |
BXGD002693 |
Snoring |
Pathological Conditions, Signs and Symptoms |
| C0040433 |
BXGD002865 |
Tooth Crowding |
Stomatognathic Diseases |
| C0078917 |
BXGD003054 |
Albinism, Ocular |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases |
| C0152423 |
BXGD003587 |
Congenital small ears |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Otorhinolaryngologic Diseases |
| C0221355 |
BXGD004447 |
Macrocephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0232466 |
BXGD004543 |
Feeding difficulties |
|
| C0233750 |
BXGD004608 |
Hysterical amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0233796 |
BXGD004619 |
Temporary Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0236795 |
BXGD004832 |
Dissociative Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0239043 |
BXGD004960 |
Difficulty chewing |
|
| C0239234 |
BXGD004974 |
Low set ears |
|
| C0239479 |
BXGD004982 |
Round face |
|
| C0262497 |
BXGD005249 |
Global Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0266060 |
BXGD005617 |
Anterior open bite |
Stomatognathic Diseases |
| C0266589 |
BXGD005698 |
Congenital ear anomaly NOS (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Otorhinolaryngologic Diseases |
| C0267048 |
BXGD005728 |
Glossoptosis |
Stomatognathic Diseases |
| C0342684 |
BXGD007525 |
Ocular albinism, type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases |
| C0399570 |
BXGD008254 |
Mandibular condyle aplasia |
Musculoskeletal Diseases; Stomatognathic Diseases |
| C0399572 |
BXGD008255 |
Hypoplasia of mandibular condyle |
Musculoskeletal Diseases; Stomatognathic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0431420 |
BXGD008688 |
Vein of Galen aneurysm |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases |
| C0431478 |
BXGD008692 |
Posteriorly rotated ear |
|
| C0431565 |
BXGD008695 |
Hamartoma of tongue |
Neoplasms; Stomatognathic Diseases |
| C0476273 |
BXGD008986 |
Respiratory distress |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0520679 |
BXGD009101 |
Sleep Apnea, Obstructive |
Respiratory Tract Diseases; Nervous System Diseases |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0750906 |
BXGD010244 |
Tactile Amnesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0750907 |
BXGD010245 |
Amnestic State |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C1269683 |
BXGD012001 |
Major Depressive Disorder |
Mental Disorders |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306710 |
BXGD012372 |
Facial asymmetry |
Pathological Conditions, Signs and Symptoms |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1845447 |
BXGD014747 |
Cupped ears (finding) |
|
| C1846460 |
BXGD014820 |
Abnormality of the outer ear |
|
| C1853406 |
BXGD015334 |
Difficulty in tongue movements |
|
| C1857486 |
BXGD015710 |
Low-set, posteriorly rotated ears |
|
| C1858120 |
BXGD015774 |
Generalized hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1860816 |
BXGD016001 |
Preauricular skin tag |
|
| C1865295 |
BXGD016307 |
Auriculo-condylar syndrome |
Otorhinolaryngologic Diseases |
| C1865302 |
BXGD016308 |
Cleft at the superior portion of the pinna |
|
| C1865304 |
BXGD016309 |
Overfolding of the superior helices |
|
| C1865305 |
BXGD016310 |
Hypoplastic superior helix |
|
| C1865313 |
BXGD016311 |
Speech articulation difficulties |
|
| C1865318 |
BXGD016312 |
Abnormality of the temporomandibular joint |
|
| C1866231 |
BXGD016388 |
Full cheeks |
|
| C1876185 |
BXGD016564 |
Dysgnathia complex |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C4021376 |
BXGD020617 |
Cleft helix |
|
| C4021380 |
BXGD020619 |
Abnormality of the crus of the helix |
|
| C4022171 |
BXGD020891 |
Periauricular skin pits |
|
| C4024626 |
BXGD021349 |
Aplasia/Hypoplasia of the external ear |
|
| C4025323 |
BXGD021645 |
Postauricular skin tag |
|
| C4551488 |
BXGD023314 |
Bifid uvula |
|
| C4551996 |
BXGD023471 |
Auriculocondylar syndrome 1 |
Otorhinolaryngologic Diseases |