Human Disease Ontology
1924 terms(s) returned
| Term Type: | Record: 1601 to 1650 of 1924 Records | Page: 33 of 39, First Previous Next Last | Show Records Per Page |
- congenital nongoitrous hypothyroidism 1
- congenital nongoitrous hypothyroidism 2
- congenital nongoitrous hypothyroidism 3
- congenital nongoitrous hypothyroidism 4
- congenital nongoitrous hypothyroidism 5
- congenital nongoitrous hypothyroidism 6
- congenital nongoitrous hypothyroidism 7
- congenital nongoitrous hypothyroidism 8
- congenital nongoitrous hypothyroidism 9
- congenital nonspherocytic hemolytic anemia
- congenital nonspherocytic hemolytic anemia 1
- congenital nonspherocytic hemolytic anemia 10
- congenital nonspherocytic hemolytic anemia 2
- congenital nonspherocytic hemolytic anemia 3
- congenital nonspherocytic hemolytic anemia 4
- congenital nonspherocytic hemolytic anemia 5
- congenital nonspherocytic hemolytic anemia 6
- congenital nonspherocytic hemolytic anemia 7
- congenital nonspherocytic hemolytic anemia 8
- congenital nonspherocytic hemolytic anemia 9
- congenital nystagmus
- congenital nystagmus 1
- congenital nystagmus 2
- congenital nystagmus 3
- congenital nystagmus 5
- congenital nystagmus 6
- congenital nystagmus 7
- congenital ptosis
- congenital secretory chloride diarrhea 1
- congenital secretory sodium diarrhea 3
- congenital secretory sodium diarrhea 8
- congenital stationary night blindness
- congenital stationary night blindness 1A
- congenital stationary night blindness 1B
- congenital stationary night blindness 1C
- congenital stationary night blindness 1D
- congenital stationary night blindness 1E
- congenital stationary night blindness 1F
- congenital stationary night blindness 1G
- congenital stationary night blindness 1H
- congenital stationary night blindness 2A
- congenital stationary night blindness autosomal dominant 1
- congenital stationary night blindness autosomal dominant 2
- congenital stationary night blindness autosomal dominant 3
- congenital stromal corneal dystrophy
- congenital structural myopathy
- congenital sucrase-isomaltase deficiency
- congenital symblepharon
- congenital symmetric circumferential skin creases 1
- congenital symmetric circumferential skin creases 2
