Mondo Disease Ontology
5921 terms(s) returned
| Term Type: | Record: 5451 to 5500 of 5921 Records | Page: 110 of 119, First Previous Next Last | Show Records Per Page |
- autosomal dominant auditory neuropathy 1
- autosomal dominant brachyolmia
- autosomal dominant cataract
- autosomal dominant centronuclear myopathy
- autosomal dominant cerebellar ataxia
- autosomal dominant cerebellar ataxia type I
- autosomal dominant cerebellar ataxia type III
- autosomal dominant cerebellar ataxia type IV
- autosomal dominant cerebellar ataxia, deafness and narcolepsy
- autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
- autosomal dominant childhood-onset proximal spinal muscular atrophy
- autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
- autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
- autosomal dominant chondrodysplasia punctata
- 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 axonal motor neuropathy-myofibrillar myopathy syndrome
- 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
