Mondo Disease Ontology
5041 terms(s) returned
Term Type: Class | Record: 4251 to 4300 of 5041 Records | Page: 86 of 101, First Previous Next Last | Show Records Per Page |
- congenital myasthenic syndrome 8
- congenital myasthenic syndrome 9
- congenital myasthenic syndrome with tubular aggregates
- congenital myopathy
- congenital myopathy 10b, mild variant
- congenital myopathy 11
- congenital myopathy 15
- congenital myopathy 18
- congenital myopathy 20
- congenital myopathy 21 with early respiratory failure
- congenital myopathy 22A, classic
- congenital myopathy 22B, severe fetal
- congenital myopathy 23
- congenital myopathy 2b, severe infantile, autosomal recessive
- congenital myopathy 2c, severe infantile, autosomal dominant
- congenital myopathy 4A, autosomal dominant
- congenital myopathy 4B, autosomal recessive
- congenital myopathy 7A, myosin storage, autosomal dominant
- congenital myopathy with internal nuclei and atypical cores
- congenital myopathy with myasthenic-like onset
- congenital myopathy with reduced type 2 muscle fibers
- congenital myopathy, Paradas type
- congenital myopathy, dog
- congenital myopathy, goat
- congenital myopathy, non-human animal
- congenital myotonic dystrophy
- congenital narrowing of cervical spinal canal
- congenital nasal pyriform aperture stenosis with holoprosencephaly
- congenital nephrotic syndrome, Finnish type
- congenital nervous system disorder
- congenital nervous system disorder, non-human animal
- congenital neuronal ceroid lipofuscinosis
- congenital neutropenia-myelofibrosis-nephromegaly syndrome
- congenital non-bullous ichthyosiform erythroderma
- congenital non-communicating hydrocephalus
- congenital nongoitrous hypothryoidism 3
- congenital nongoitrous hypothryoidism 6
- congenital nonhemolytic jaundice
- congenital nonspherocytic hemolytic anemia
- congenital nystagmus
- congenital nystagmus, dog
- congenital nystagmus, non-human animal
- congenital oculomotor nerve palsy
- congenital optic disk excavation
- congenital or acquired
- congenital or early infantile CACH syndrome
- congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
- congenital pancreatic cyst
- congenital panfollicular nevus
- congenital partial agenesis of pericardium