Mondo Disease Ontology
1825 terms(s) returned
| Term Type: | Record: 951 to 1000 of 1825 Records | Page: 20 of 37, First Previous Next Last | Show Records Per Page |
- leprosy, susceptibility to, 3
- leprosy, susceptibility to, 4
- leprosy, susceptibility to, 5
- leprosy, susceptibility to, 6
- leptomeningeal melanoma
- leptomeningeal sarcoma
- leptomeninx
- leptomyelolipoma
- lepton
- leptospirosis
- lesion of sciatic nerve
- lessel-kubisch syndrome
- lethal Kniest-like dysplasia
- lethal Larsen-like syndrome
- lethal acantholytic epidermolysis bullosa
- lethal acrodermatitis, dog
- lethal acrodermatitis, non-human animal
- lethal arteriopathy syndrome due to fibulin-4 deficiency
- lethal arthrogryposis syndrome, cattle
- lethal arthrogryposis syndrome, non-human animal
- lethal arthrogryposis-anterior horn cell disease syndrome
- lethal chondrodysplasia, Seller type
- lethal congenital contracture syndrome
- lethal congenital contracture syndrome 1
- lethal congenital contracture syndrome 11
- lethal congenital contracture syndrome 2
- lethal congenital contracture syndrome 3
- lethal congenital contracture syndrome 4
- lethal congenital contracture syndrome 6
- lethal congenital contracture syndrome 7
- lethal congenital contracture syndrome 8
- lethal congenital contracture syndrome 9
- lethal congenital glycogen storage disease of heart
- lethal faciocardiomelic dysplasia
- lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
- lethal hemolytic anemia-genital anomalies syndrome
- lethal hydranencephaly-diaphragmatic hernia syndrome
- lethal infantile mitochondrial myopathy
- lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
- lethal multi-organ developmental dysplasia, cattle
- lethal multi-organ developmental dysplasia, non-human animal
- lethal multiple pterygium syndrome
- lethal occipital encephalocele-skeletal dysplasia syndrome
- lethal omphalocele-cleft palate syndrome
- lethal osteosclerotic bone dysplasia
- lethal polymalformative syndrome, Boissel type
- lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation
- lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster
- lethal recessive chondrodysplasia
- lethal short-limb skeletal dysplasia, Al Gazali type
