Mondo Disease Ontology
5519 terms(s) returned
| Term Type: | Record: 4601 to 4650 of 5519 Records | Page: 93 of 111, First Previous Next Last | Show Records Per Page |
- congenital limb malformation
- congenital lipoid adrenal hyperplasia due to STAR deficency
- congenital liver fibrosis, PKHD1-related, horse
- congenital lobar emphysema
- congenital macroglossia
- congenital malabsorptive diarrhea 4
- congenital mast cell tumor, cattle
- congenital mast cell tumor, non-human animal
- congenital megacalycosis
- congenital megaprepuce
- congenital melanoma, non-human animal
- congenital melanoma, pig
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
- congenital merosin-deficient muscular dystrophy 1A
- congenital merosin-deficient muscular dystrophy, domestic cat
- congenital merosin-deficient muscular dystrophy, non-human animal
- congenital mesoblastic nephroma
- congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
- congenital microcoria
- congenital microgastria
- congenital mitral malformation
- congenital mitral stenosis
- congenital mitral valve agenesis
- congenital mitral valve insufficiency
- congenital mitral valve insufficiency and/or stenosis
- congenital multicore myopathy with external ophthalmoplegia
- congenital mumps
- congenital muscular dystonia SLC6A5-related, cattle
- congenital muscular dystonia, ATP2A1-related, cattle
- congenital muscular dystrophy
- congenital muscular dystrophy 1B
- congenital muscular dystrophy caused by variation in POMGNT2
- congenital muscular dystrophy due to LMNA mutation
- congenital muscular dystrophy due to integrin alpha-7 deficiency
- congenital muscular dystrophy with cataracts and intellectual disability
- congenital muscular dystrophy with hyperlaxity
- congenital muscular dystrophy with intellectual disability
- congenital muscular dystrophy with intellectual disability and severe epilepsy
- congenital muscular dystrophy without intellectual disability
- congenital muscular dystrophy, LAMA2-related, dog
- congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome
- congenital myasthenic syndrome
- congenital myasthenic syndrome 10
- congenital myasthenic syndrome 11
- congenital myasthenic syndrome 12
- congenital myasthenic syndrome 13
- congenital myasthenic syndrome 14
- congenital myasthenic syndrome 15
- congenital myasthenic syndrome 16
