Mondo Disease Ontology
5519 terms(s) returned
| Term Type: | Record: 4801 to 4850 of 5519 Records | Page: 97 of 111, First Previous Next Last | Show Records Per Page |
- congenital stationary night blindness autosomal dominant 3
- congenital stationary night blindness, LRIT3-related, dog
- congenital stationary night blindness, TRPM1-related, horse
- congenital stenosis of cervical medullary canal
- congenital stenosis of the inferior vena cava
- congenital stromal corneal dystrophy
- congenital structural myopathy
- congenital subglottic stenosis
- congenital sucrase-isomaltase deficiency
- congenital sucrase-isomaltase deficiency with minimal starch tolerance
- congenital sucrase-isomaltase deficiency with starch and lactose intolerance
- congenital sucrase-isomaltase deficiency with starch intolerance
- congenital sucrase-isomaltase deficiency without starch intolerance
- congenital sucrase-isomaltase deficiency without sucrose intolerance
- congenital supravalvular mitral ring
- congenital symblepharon
- congenital syphilis
- congenital systemic arteriovenous fistula
- congenital temporomandibular joint ankylosis
- congenital thrombotic thrombocytopenic purpura
- congenital total pulmonary venous return anomaly
- congenital toxoplasmosis
- congenital tracheal stenosis
- congenital tracheomalacia
- congenital tricuspid malformation
- congenital tricuspid stenosis
- congenital trigeminal anesthesia
- congenital unguarded mitral orifice
- congenital unilateral hypoplasia of depressor anguli oris
- congenital unilateral pulmonary hypoplasia
- congenital urachal anomaly
- congenital vagal hyperreflexivity
- congenital varicella syndrome
- congenital vascular malformation
- congenital velopharyngeal incompetence
- congenital vertebral-cardiac-renal anomalies syndrome
- congenital vertical talus
- congenital vertical talus, bilateral
- congenital vertical talus, unilateral
- congenital vitamin K-dependent coagulation factors deficiency
- congenital vitreoretinal dysplasia
- congenital-onset Steinert myotonic dystrophy
- congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements
- congenitally corrected transposition of the great arteries
- congenitally short costocoracoid ligament
- congenitally uncorrected transposition of the great arteries with cardiac malformation
- congenitally uncorrected transposition of the great arteries with coarctation
- congential hepatic fibrosis, dog
- congential hepatic fibrosis, non-human animal
- congestive heart failure
