Experimental Factor Ontology
376 terms(s) returned
Term Type: | Record: 151 to 200 of 376 Records | Page: 4 of 8, First Previous Next Last | Show Records Per Page |
- lethal congenital contracture syndrome
- lethal congenital contracture syndrome 1
- lethal congenital contracture syndrome 2
- lethal congenital contracture syndrome 3
- lethal congenital glycogen storage disease of heart
- lethal faciocardiomelic dysplasia
- lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
- lethal hemolytic anemia-genital anomalies syndrome
- lethal infantile mitochondrial myopathy
- 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 recessive chondrodysplasia
- lethal short-limb skeletal dysplasia, Al Gazali type
- leukemia, acute lymphoblastic, susceptibility to, 3
- leukemia, acute myeloid, susceptibility to
- leukemia, acute, X-linked
- leukocyte adhesion deficiency
- leukocyte adhesion deficiency 1
- leukocyte adhesion deficiency 3
- leukocyte adhesion deficiency type II
- leukocyte disorder
- leukodystrophy
- leukodystrophy and acquired microcephaly with or without dystonia;
- leukodystrophy, childhood-onset, remitting
- leukodystrophy, hypomyelinating, 15
- leukodystrophy, hypomyelinating, 17
- leukodystrophy, hypomyelinating, 20
- leukodystrophy, hypomyelinating, 22
- leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy
- leukodystrophy, hypomyelinating, 26, with chondrodysplasia
- leukoencephalopathy with bilateral anterior temporal lobe cysts
- leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
- leukoencephalopathy with calcifications and cysts
- leukoencephalopathy with mild cerebellar ataxia and white matter edema
- leukoencephalopathy with vanishing white matter
- leukoencephalopathy with vanishing white matter 1
- leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome
- leukoencephalopathy, diffuse hereditary, with spheroids 1
- leukoencephalopathy, hereditary diffuse, with spheroids
- leukoencephalopathy, hereditary diffuse, with spheroids 2
- leukoencephalopathy, megalencephalic
- leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome
- leukoencephalopathy, porphyria-related
- leukoencephalopathy, progressive, infantile-onset, with or without deafness
- leukoencephalopathy, progressive, with ovarian failure
- leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome
- leukoencephalopathy-palmoplantar keratoderma syndrome