Mondo Disease Ontology
5958 terms(s) returned
| Term Type: | Record: 5501 to 5550 of 5958 Records | Page: 111 of 120, First Previous Next Last | Show Records Per Page |
- 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
- autosomal dominant distal renal tubular acidosis
- autosomal dominant dopa-responsive dystonia
- autosomal dominant epidermolytic ichthyosis
- autosomal dominant epilepsy with auditory features
- autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome
- autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- autosomal dominant hyperinsulinism due to SUR1 deficiency
- autosomal dominant hypocalcemia
- autosomal dominant hypocalcemia 1
- autosomal dominant hypocalcemia 2
- autosomal dominant hypohidrotic ectodermal dysplasia
- autosomal dominant hypophosphatemic rickets
- autosomal dominant ichthyosis vulgaris
- autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
- autosomal dominant intermediate Charcot-Marie-Tooth disease
- autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
- autosomal dominant keratitis
- autosomal dominant keratitis-ichthyosis-hearing loss syndrome
- autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)
- autosomal dominant limb-girdle muscular dystrophy type 1E (DES)
- autosomal dominant limb-girdle muscular dystrophy type 1F
- autosomal dominant limb-girdle muscular dystrophy type 1G
- autosomal dominant limb-girdle muscular dystrophy type 1H
- autosomal dominant macrothrombocytopenia
- autosomal dominant medullary cystic kidney disease with or without hyperuricemia
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- autosomal dominant mitochondrial myopathy with exercise intolerance
- autosomal dominant myoglobinuria
- autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome
- autosomal dominant nebulin-related myopathy
- autosomal dominant nephritis, dog
- autosomal dominant nocturnal frontal lobe epilepsy
- autosomal dominant nocturnal frontal lobe epilepsy 1
- autosomal dominant nocturnal frontal lobe epilepsy 2
- autosomal dominant nocturnal frontal lobe epilepsy 3
- autosomal dominant nocturnal frontal lobe epilepsy 4
- autosomal dominant nocturnal frontal lobe epilepsy 5
- autosomal dominant non-nuclear cataract
