Experimental Factor Ontology
8052 terms(s) returned
| Term Type: | Record: 401 to 450 of 8052 Records | Page: 9 of 162, First Previous Next Last | Show Records Per Page |
- obsolete adrenal/paraganglial tumor
- obsolete adult hypophosphatasia
- obsolete aggrecan-related bone disorder
- obsolete aging
- obsolete aleukemic mast cell leukemia
- obsolete alpha-crystallinopathy
- obsolete alpha-thalassemia and related diseases
- obsolete alpha-thalassemia-related diseases
- obsolete anomaly of puberty or/and menstrual cycle of genetic origin
- obsolete anomaly of the secretory and excretory apparatus of the lacrimal system
- obsolete anophthalmia-microphthalmia syndrome
- obsolete antenatal Bartter syndrome
- obsolete aortic malformation
- obsolete apolipoprotein A-I deficiency
- obsolete appendix goblet cell carcinoid
- obsolete aromatic compound biosynthetic process
- obsolete asymptomatic COVID-19 infection
- obsolete atrioventricular valve anomaly
- obsolete atypical chronic myeloid leukemia
- obsolete autosomal dominant Opitz G/BBB syndrome
- obsolete autosomal dominant diffuse mutilating palmoplantar keratoderma
- obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
- obsolete autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
- obsolete autosomal dominant hereditary axonal motor and sensory neuropathy
- obsolete autosomal dominant hereditary demyelinating motor and sensory neuropathy
- obsolete autosomal dominant hereditary sensory and autonomic neuropathy
- obsolete autosomal dominant isolated diffuse palmoplantar keratoderma
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
- obsolete autosomal dominant medullary cystic kidney disease with hyperuricemia
- obsolete autosomal dominant neovascular inflammatory vitreoretinopathy
- obsolete autosomal dominant proximal spinal muscular atrophy
- obsolete autosomal dominant pure spastic paraplegia
- obsolete autosomal dominant secondary polycythemia
- obsolete autosomal ichthyosis syndrome
- obsolete autosomal monosomy
- obsolete autosomal recessive Emery-Dreifuss muscular dystrophy
- obsolete autosomal recessive Stickler syndrome
- obsolete autosomal recessive axonal hereditary motor and sensory neuropathy
- obsolete autosomal recessive complex spastic paraplegia
- obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
- obsolete autosomal recessive disease with focal palmoplantar keratoderma as a major feature
- obsolete autosomal recessive distal myopathy
- obsolete autosomal recessive hereditary demyelinating motor and sensory neuropathy
- obsolete autosomal recessive hereditary sensory and autonomic neuropathy
- obsolete autosomal recessive isolated diffuse palmoplantar keratoderma
- obsolete autosomal recessive limb-girdle muscular dystrophy type 2R
- obsolete autosomal recessive lymphoproliferative disease
- obsolete autosomal recessive optic atrophy
- obsolete autosomal recessive pure spastic paraplegia
- obsolete autosomal thrombocytopenia with normal platelets
