Human Disease Ontology
2240 terms(s) returned
| Term Type: | Record: 1651 to 1700 of 2240 Records | Page: 34 of 45, First Previous Next Last | Show Records Per Page |
- autosomal dominant auditory neuropathy 1
- autosomal dominant auditory neuropathy 3
- autosomal dominant autoinflammation, panniculitis, and dermatosis syndrome
- autosomal dominant beta thalassemia
- autosomal dominant brain small vessel disease 2A
- autosomal dominant centronuclear myopathy
- autosomal dominant cerebellar ataxia
- autosomal dominant cerebellar ataxia, deafness and narcolepsy
- autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1
- autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 2
- autosomal dominant chondrodysplasia punctata
- autosomal dominant congenital deafness with onychodystrophy
- autosomal dominant craniodiaphyseal dysplasia
- autosomal dominant craniometaphyseal dysplasia
- autosomal dominant cutis laxa
- autosomal dominant cutis laxa 1
- autosomal dominant cutis laxa 2
- autosomal dominant cutis laxa 3
- autosomal dominant disease
- autosomal dominant distal hereditary motor neuronopathy
- autosomal dominant distal hereditary motor neuronopathy 1
- autosomal dominant distal hereditary motor neuronopathy 10
- autosomal dominant distal hereditary motor neuronopathy 11
- autosomal dominant distal hereditary motor neuronopathy 12
- autosomal dominant distal hereditary motor neuronopathy 13
- autosomal dominant distal hereditary motor neuronopathy 14
- autosomal dominant distal hereditary motor neuronopathy 15
- autosomal dominant distal hereditary motor neuronopathy 2
- autosomal dominant distal hereditary motor neuronopathy 3
- autosomal dominant distal hereditary motor neuronopathy 4
- autosomal dominant distal hereditary motor neuronopathy 5
- autosomal dominant distal hereditary motor neuronopathy 6
- autosomal dominant distal hereditary motor neuronopathy 7
- autosomal dominant distal hereditary motor neuronopathy 8
- autosomal dominant distal hereditary motor neuronopathy 9
- autosomal dominant dyskeratosis congenita 1
- autosomal dominant dyskeratosis congenita 2
- autosomal dominant dyskeratosis congenita 3
- autosomal dominant dyskeratosis congenita 4
- autosomal dominant dyskeratosis congenita 6
- autosomal dominant dystrophic epidermolysis bullosa
- autosomal dominant familial visceral neuropathy
- autosomal dominant hyaline body myopathy
- autosomal dominant hyper-IgE syndrome 1 with recurrent infections
- autosomal dominant hypocalcemia
- autosomal dominant hypocalcemia 1
- autosomal dominant hypocalcemia 2
- autosomal dominant hypophosphatemic rickets
- autosomal dominant inheritance
- autosomal dominant intellectual developmental disorder
