Mondo Disease Ontology
5946 terms(s) returned
| Term Type: | Record: 5451 to 5500 of 5946 Records | Page: 110 of 119, First Previous Next Last | Show Records Per Page |
- autopod skin
- autopodial extension
- autopodial skeleton
- autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, non-human animal
- autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, pig
- autosomal agammaglobulinemia
- autosomal anomaly
- autosomal dominant Aarskog syndrome
- autosomal dominant Alport syndrome
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
- autosomal dominant Charcot-Marie-Tooth disease type 2K
- autosomal dominant Charcot-Marie-Tooth disease type 2M
- autosomal dominant Charcot-Marie-Tooth disease type 2W
- autosomal dominant Ehlers-Danlos syndrome, vascular type
- autosomal dominant Emery-Dreifuss muscular dystrophy
- autosomal dominant Kenny-Caffey syndrome
- autosomal dominant Parkinson disease 1
- autosomal dominant Parkinson disease 4
- autosomal dominant Parkinson disease 8
- autosomal dominant Robinow syndrome
- autosomal dominant Robinow syndrome 1
- autosomal dominant Robinow syndrome 2
- autosomal dominant Robinow syndrome 3
- autosomal dominant aplasia and myelodysplasia
- autosomal dominant auditory neuropathy 1
- autosomal dominant brachyolmia
- autosomal dominant cataract
- autosomal dominant centronuclear myopathy
- autosomal dominant cerebellar ataxia
- autosomal dominant cerebellar ataxia type I
- autosomal dominant cerebellar ataxia type III
- autosomal dominant cerebellar ataxia type IV
- autosomal dominant cerebellar ataxia, deafness and narcolepsy
- autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
- autosomal dominant childhood-onset proximal spinal muscular atrophy
- autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
- autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
- autosomal dominant chondrodysplasia punctata
- autosomal dominant coarctation of aorta
- autosomal dominant combined immunodeficiency due to ERBIN deficiency
- autosomal dominant combined immunodeficiency due to partial IL6ST deficiency
- autosomal dominant complex spastic paraplegia
- autosomal dominant complex spastic paraplegia type 9B
- autosomal dominant cutis laxa
- autosomal dominant cystinuria, SLC3A1-related, dog
- autosomal dominant cystinuria, SLC7A9-related, dog
- autosomal dominant deafness - onychodystrophy syndrome
- autosomal dominant disease
- autosomal dominant distal myopathy
