Mondo Disease Ontology
5946 terms(s) returned
| Term Type: | Record: 5651 to 5700 of 5946 Records | Page: 114 of 119, First Previous Next Last | Show Records Per Page |
- 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
- 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
- autosomal recessive degenerative and progressive cerebellar ataxia
- autosomal recessive disease
- autosomal recessive distal osteolysis syndrome
- autosomal recessive distal renal tubular acidosis
- autosomal recessive distal spinal muscular atrophy 1
- autosomal recessive distal spinal muscular atrophy 2
- autosomal recessive distal titinopathy
- autosomal recessive dyskeratosis congenita 4
- autosomal recessive early-onset Parkinson disease 23
- autosomal recessive early-onset Parkinson disease 6
- autosomal recessive early-onset Parkinson disease 7
- autosomal recessive epidermolytic ichthyosis
- autosomal recessive extra-oral halitosis
