Mondo Disease Ontology
5908 terms(s) returned
| Term Type: | Record: 5601 to 5650 of 5908 Records | Page: 113 of 119, First Previous Next Last | Show Records Per Page |
- 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-blindness-deafness syndrome
- 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
- autosomal recessive congenital ichthyosis 3
- autosomal recessive congenital ichthyosis 4A
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive congenital ichthyosis 5
- autosomal recessive congenital ichthyosis 6
- autosomal recessive congenital ichthyosis 7
- autosomal recessive congenital ichthyosis 8
- autosomal recessive congenital ichthyosis 9
- autosomal recessive cutis laxa type 1
- autosomal recessive cutis laxa type 2
- autosomal recessive cutis laxa type 2, classic type
- autosomal recessive cutis laxa type 2A
- autosomal recessive cutis laxa type 2B
- autosomal recessive cutis laxa type 2C
- autosomal recessive cutis laxa type 2D
- autosomal recessive cystinuria, SLC3A1-related, dog
