Experimental Factor Ontology
11043 terms(s) returned
| Term Type: | Record: 951 to 1000 of 11043 Records | Page: 20 of 221, First Previous Next Last | Show Records Per Page |
- obsolete partial autosomal monosomy
- obsolete partial autosomal trisomy/tetrasomy
- obsolete partial duplication of the long arm of chromosome 11
- obsolete partial duplication of the long arm of chromosome 13
- obsolete partial trisomy of the short arm of chromosome 9
- obsolete patellar dysostosis
- obsolete peeling skin syndrome type B
- obsolete penile fibromatosis
- obsolete periodic fever, menstrual cycle-dependent
- obsolete periodic paralysis with transient compartment-like syndrome
- obsolete peripheral neuron
- obsolete perlecan-related bone disorder
- obsolete persistent combined dystonia
- obsolete pigmented conjunctival lesion
- obsolete pigmented palpebral tumor
- obsolete pigmented villonodular synovitis
- obsolete plastid part
- obsolete polyglucosan body myopathy type 1
- obsolete polygonal cell
- obsolete polysome
- obsolete polysomy of X chromosome
- obsolete pontine autosomal dominant microangiopathy with leukoencephalopathy
- obsolete posterior fossa malformation
- obsolete precancerous lesion of palpebral epidermis
- obsolete prenatal benign hypophosphatasia
- obsolete presynaptic congenital myasthenic syndrome
- obsolete primary bone dysplasia with increased bone density
- obsolete primary bone dysplasia with multiple joint dislocations
- obsolete primary congenital hypothyroidism
- obsolete primary glomerular disease
- obsolete primary hereditary glaucoma
- obsolete primary immunodeficiency due to a defect in adaptive immunity
- obsolete primary immunodeficiency due to a genetic defect in innate immunity
- obsolete primary lipodystrophy
- obsolete primary myoclonus
- obsolete primary parathyroid hyperplasia
- obsolete primary qualitative or quantitative defects of alpha-dystroglycan
- obsolete primary renal tubular acidosis
- obsolete primary short bowel syndrome
- obsolete processed material
- obsolete progressive cerebello-cerebral atrophy
- obsolete proliferative vitreoretinopathy
- obsolete protein glycosylation
- obsolete protein glycosylation in endoplasmic reticulum
- obsolete pulmonary arteriovenous malformation
- obsolete pure or complex X-linked spastic paraplegia
- obsolete pure or complex autosomal dominant spastic paraplegia
- obsolete pure or complex autosomal recessive spastic paraplegia
- obsolete putative T-complex protein 10A homolog (human)
- obsolete putative uncharacterized protein TXNRD3NB (human)
