Mondo Disease Ontology
5753 terms(s) returned
| Term Type: | Record: 1151 to 1200 of 5753 Records | Page: 24 of 116, First Previous Next Last | Show Records Per Page |
- 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 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
- obsolete autosomal recessive pure spastic paraplegia
- obsolete autosomal recessive spastic paraplegia type 82
- obsolete autosomal recessive spastic paraplegia type 83
- obsolete autosomal recessive spastic paraplegia type 84
- obsolete autosomal recessive spastic paraplegia type 85
- obsolete autosomal recessive spastic paraplegia type 86
- obsolete autosomal recessive spastic paraplegia type 87
- obsolete autosomal thrombocytopenia with normal platelets
- obsolete autosomal trisomy
- obsolete autosomal uniparental disomy
- obsolete avascular necrosis of genetic origin
- obsolete avian influenza
- obsolete axial osteomalacia
- obsolete axon part
- obsolete axonal hereditary motor and sensory neuropathy
- obsolete babesiosis
