Mondo Disease Ontology
5921 terms(s) returned
| Term Type: | Record: 5401 to 5450 of 5921 Records | Page: 109 of 119, First Previous Next Last | Show Records Per Page |
- autoinflammatory syndrome of childhood
- autoinflammatory syndrome with immunodeficiency
- autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- autoinflammatory syndrome, familial, Behcet-like
- autoinflammatory syndrome, familial, Behcet-like 1
- autoinflammatory syndrome, familial, X-linked, Behcet-like 2
- autoinflammatory syndrome due to TBK1 deficiency
- autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency
- autonomic dysreflexia
- autonomic facial cephalgia
- autonomic ganglion
- autonomic nerve
- autonomic nerve plexus
- autonomic nervous system
- autonomic nervous system benign neoplasm
- autonomic nervous system disorder
- autonomic nervous system neoplasm
- autonomic neuron
- autonomic neuropathy
- autopod bone
- autopod cartilage
- autopod endochondral element
- autopod hair
- autopod joint
- autopod region
- 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
