Mondo Disease Ontology
5908 terms(s) returned
| Term Type: | Record: 5551 to 5600 of 5908 Records | Page: 112 of 119, First Previous Next Last | Show Records Per Page |
- autosomal dominant nonsyndromic hearing loss 68
- autosomal dominant nonsyndromic hearing loss 69
- autosomal dominant nonsyndromic hearing loss 7
- autosomal dominant nonsyndromic hearing loss 70
- autosomal dominant nonsyndromic hearing loss 9
- autosomal dominant oculocutaneous albinism
- autosomal dominant omodysplasia
- autosomal dominant optic atrophy
- autosomal dominant optic atrophy and peripheral neuropathy
- autosomal dominant optic atrophy plus syndrome
- autosomal dominant optic atrophy, classic form
- autosomal dominant osteopetrosis
- autosomal dominant osteopetrosis 1
- autosomal dominant osteopetrosis 2
- autosomal dominant osteosclerosis, Worth type
- autosomal dominant palmoplantar keratoderma and congenital alopecia
- autosomal dominant polycystic kidney disease
- autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- autosomal dominant polycystic liver disease
- autosomal dominant popliteal pterygium syndrome
- autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome
- autosomal dominant primary microcephaly
- autosomal dominant prognathism
- autosomal dominant progressive external ophthalmoplegia
- autosomal dominant progressive nephropathy with hypertension
- autosomal dominant progressive retinal atrophy, RHO-related, dog
- autosomal dominant proximal renal tubular acidosis
- autosomal dominant pseudohypoaldosteronism type 1
- autosomal dominant rhegmatogenous retinal detachment
- autosomal dominant sensory ataxia 1
- autosomal dominant severe congenital neutropenia
- autosomal dominant sideroblastic anemia
- autosomal dominant slowed nerve conduction velocity
- autosomal dominant spastic ataxia
- autosomal dominant spastic paraplegia type 9
- autosomal dominant spondylocostal dysostosis
- autosomal dominant striatal neurodegeneration type 1
- autosomal dominant syndromic intellectual disability
- autosomal dominant titinopathy
- autosomal dominant trichoodontoonychodysplasia-syndactyly
- autosomal dominant vibratory urticaria
- autosomal dominant vitreoretinochoroidopathy
- autosomal dominant wooly hair
- autosomal dwarfism, chicken
- autosomal dwarfism, non-human animal
- autosomal erythropoietic protoporphyria
- autosomal genetic disease
- autosomal recessive Alport syndrome
- autosomal recessive Ehlers-Danlos syndrome, vascular type
- autosomal recessive Kenny-Caffey syndrome
