Mondo Disease Ontology
2326 terms(s) returned
| Term Type: | Record: 1851 to 1900 of 2326 Records | Page: 38 of 47, First Previous Next Last | Show Records Per Page |
- neuronal intestinal dysplasia, type B
- neuronal intranuclear inclusion disease
- neuronal receptor cell
- neuronal vacuolar disorder, dog
- neuronal vacuolar disorder, non-human animal
- neuronitis
- neuronopathy, distal hereditary motor, autosomal dominant
- neuronopathy, distal hereditary motor, autosomal dominant 1
- neuronopathy, distal hereditary motor, autosomal dominant 10
- neuronopathy, distal hereditary motor, autosomal dominant 11
- neuronopathy, distal hereditary motor, autosomal dominant 15
- neuronopathy, distal hereditary motor, autosomal dominant 8
- neuronopathy, distal hereditary motor, autosomal recessive
- neuronopathy, distal hereditary motor, autosomal recessive 10
- neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity
- neuronopathy, distal hereditary motor, autosomal recessive 3
- neuronopathy, distal hereditary motor, autosomal recessive 4
- neuronopathy, distal hereditary motor, autosomal recessive 5
- neuronopathy, distal hereditary motor, autosomal recessive 7
- neuronopathy, distal hereditary motor, autosomal recessive 8
- neuronopathy, distal hereditary motor, autosomal recessive 9
- neuronopathy, distal hereditary motor, type 2A
- neuronopathy, distal hereditary motor, type 2B
- neuronopathy, distal hereditary motor, type 2C
- neuronopathy, distal hereditary motor, type 2D
- neuronopathy, distal hereditary motor, type 5
- neuronopathy, distal hereditary motor, type 5A
- neuronopathy, distal hereditary motor, type 5B
- neuronopathy, distal hereditary motor, type 5C
- neuronopathy, distal hereditary motor, type 7A
- neuronopathy, distal hereditary motor, type 7B
- neuronopathy, distal hereditary motor, type 9
- neuroocular syndrome
- neuroocular syndrome 1
- neurooculocardiogenitourinary syndrome
- neurooculorenal syndrome
- neuropathy and feather color dilution, Northern goshawk
- neuropathy and feather color dilution, non-human animal
- neuropathy with hearing impairment
- neuropathy with splayed forelimbs, UCHL1-related, cattle
- neuropathy, congenital hypomelinating
- neuropathy, congenital hypomyelinating, 2
- neuropathy, congenital hypomyelinating, 3
- neuropathy, congenital, with arthrogryposis multiplex
- neuropathy, hereditary motor and sensory, type 6A
- neuropathy, hereditary motor and sensory, type 6B
- neuropathy, hereditary motor and sensory, type VIc, with optic atrophy
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
- neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia
- neuropathy, hereditary sensory and autonomic, type 1A
