Mondo Disease Ontology
5944 terms(s) returned
| Term Type: | Record: 1201 to 1250 of 5944 Records | Page: 25 of 119, First Previous Next Last | Show Records Per Page |
- obsolete autosomal dominant hereditary sensory and autonomic neuropathy
- obsolete autosomal dominant isolated diffuse palmoplantar keratoderma
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1E
- obsolete autosomal dominant macrothrombocytopenia TUBB1-related
- obsolete autosomal dominant medullary cystic kidney disease with hyperuricemia
- obsolete autosomal dominant medullary cystic kidney disease without hyperuricemia
- obsolete autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency
- obsolete autosomal dominant neovascular inflammatory vitreoretinopathy
- obsolete autosomal dominant nocturnal frontal lobe epilepsy
- obsolete autosomal dominant nonsyndromic hearing loss 52
- obsolete autosomal dominant proximal spinal muscular atrophy
- obsolete autosomal dominant pure spastic paraplegia
- obsolete autosomal dominant secondary polycythemia
- obsolete autosomal dominant spastic paraplegia type 80
- obsolete autosomal ichthyosis syndrome
- obsolete autosomal ichthyosis syndrome with fatal disease course
- obsolete autosomal ichthyosis syndrome with other associated signs
- obsolete autosomal ichthyosis syndrome with other associated signs
- obsolete autosomal ichthyosis syndrome with prominent hair abnormalities
- obsolete autosomal ichthyosis syndrome with prominent neurologics signs
- obsolete autosomal monosomy
- obsolete autosomal recessive Emery-Dreifuss muscular dystrophy
- obsolete autosomal recessive Stickler syndrome
- obsolete autosomal recessive axonal hereditary motor and sensory neuropathy
- obsolete autosomal recessive cerebellar ataxia
- obsolete autosomal recessive cerebellar ataxia due to a DNA repair defect
- obsolete autosomal recessive cerebellar ataxia-blindness-deafness syndrome
- obsolete autosomal recessive complex spastic paraplegia
- obsolete autosomal recessive disease
- obsolete autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
- obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
- obsolete autosomal recessive disease with focal palmoplantar keratoderma as a major feature
- obsolete autosomal recessive distal myopathy
- obsolete autosomal recessive extra-oral halitosis
- obsolete autosomal recessive hereditary demyelinating motor and sensory neuropathy
- obsolete autosomal recessive hereditary sensory and autonomic neuropathy
- obsolete autosomal recessive hyper-IgE syndrome
- obsolete autosomal recessive hypophosphatemic rickets
- obsolete autosomal recessive infantile hypercalcemia
- obsolete autosomal recessive isolated diffuse palmoplantar keratoderma
- obsolete autosomal recessive limb-girdle muscular dystrophy type 2R
- obsolete autosomal recessive lymphoproliferative disease
- obsolete autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency
- obsolete autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
- obsolete autosomal recessive nail dysplasia
- obsolete autosomal recessive nonsyndromic deafness 105
- obsolete autosomal recessive optic atrophy
