Mondo Disease Ontology
5924 terms(s) returned
| Term Type: | Record: 5601 to 5650 of 5924 Records | Page: 113 of 119, First Previous Next Last | Show Records Per Page |
- autosomal dominant spastic ataxia
- autosomal dominant spastic paraplegia type 9
- autosomal dominant spondylocostal dysostosis
- autosomal dominant striatal neurodegeneration type 1
- autosomal dominant syndromic intellectual disability
- autosomal dominant titinopathy
- autosomal dominant trichoodontoonychodysplasia-syndactyly
- autosomal dominant vibratory urticaria
- autosomal dominant vitreoretinochoroidopathy
- autosomal dominant wooly hair
- autosomal dwarfism, chicken
- autosomal dwarfism, non-human animal
- autosomal erythropoietic protoporphyria
- autosomal genetic disease
- autosomal recessive Alport syndrome
- autosomal recessive Ehlers-Danlos syndrome, vascular type
- autosomal recessive Kenny-Caffey syndrome
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- autosomal recessive Parkinson disease 14
- autosomal recessive Robinow syndrome
- autosomal recessive agammaglobulinemia 1
- autosomal recessive amelia
- autosomal recessive ataxia due to PEX10 deficiency
- autosomal recessive ataxia due to PEX16 deficiency
- autosomal recessive ataxia due to PEX2 deficiency
- autosomal recessive ataxia due to ubiquinone deficiency
- autosomal recessive ataxia, Beauce type
- autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
- autosomal recessive bestrophinopathy
- autosomal recessive brachyolmia
- autosomal recessive centronuclear myopathy
- autosomal recessive cerebellar ataxia
- autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
- autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
- autosomal recessive cerebellar ataxia with late-onset spasticity
- autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
- autosomal recessive cerebral atrophy
- autosomal recessive combined immunodeficiency due to IL6R deficiency
- autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
- autosomal recessive combined immunodeficiency due to partial IL6ST deficiency
- autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
- autosomal recessive complex spastic paraplegia type 9B
- autosomal recessive congenital cerebellar ataxia
- autosomal recessive congenital ichthyosis
- autosomal recessive congenital ichthyosis 1
- autosomal recessive congenital ichthyosis 10
- autosomal recessive congenital ichthyosis 11
- autosomal recessive congenital ichthyosis 2
