Mondo Disease Ontology
6020 terms(s) returned
| Term Type: | Record: 5051 to 5100 of 6020 Records | Page: 102 of 121, First Previous Next Last | Show Records Per Page |
- congenital myasthenic syndrome 17
- congenital myasthenic syndrome 18
- congenital myasthenic syndrome 19
- congenital myasthenic syndrome 1A
- congenital myasthenic syndrome 20
- congenital myasthenic syndrome 21
- congenital myasthenic syndrome 2A
- congenital myasthenic syndrome 2C
- congenital myasthenic syndrome 3A
- congenital myasthenic syndrome 3B
- congenital myasthenic syndrome 3C
- congenital myasthenic syndrome 4
- congenital myasthenic syndrome 4A
- congenital myasthenic syndrome 4B
- congenital myasthenic syndrome 4C
- congenital myasthenic syndrome 5
- congenital myasthenic syndrome 6
- congenital myasthenic syndrome 7
- congenital myasthenic syndrome 8
- congenital myasthenic syndrome 9
- congenital myasthenic syndrome with tubular aggregates
- congenital myasthenic syndrome, CHAT-related, dog
- congenital myasthenic syndrome, CHRNE-related, cattle
- congenital myasthenic syndrome, CHRNE-related, dog
- congenital myasthenic syndrome, COLQ-related, dog
- 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 25
- congenital myopathy 26
- congenital myopathy 27
- congenital myopathy 28 with rigid spine
- congenital myopathy 29 with contractures
- congenital myopathy 2a, typical, autosomal dominant
- 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 fiber-type disproportion, dog
- congenital myopathy with fiber-type disproportion, non-human animal
- congenital myopathy with internal nuclei and atypical cores
- congenital myopathy with myasthenic-like onset
