Mondo Disease Ontology
134 terms(s) returned
Term Type: | Record: 51 to 100 of 134 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- Joubert syndrome 37
- Joubert syndrome 38
- Joubert syndrome 39
- Joubert syndrome 40
- Joubert syndrome 5
- Joubert syndrome 6
- Joubert syndrome 7
- Joubert syndrome 8
- Joubert syndrome 9
- Joubert syndrome and related disorders
- Joubert syndrome with Jeune asphyxiating thoracic dystrophy
- Joubert syndrome with ocular defect
- Joubert syndrome with oculorenal defect
- Joubert syndrome with renal defect
- Juberg-Hayward syndrome
- Judge Misch wright syndrome
- Jumping Frenchmen of Maine
- janus kinase-3 deficiency
- jaundice, familial obstructive, of infancy
- jaw cancer
- jaw fracture
- jaw-winking syndrome
- jejunal adenocarcinoma
- jejunal atresia with renal adysplasia
- jejunal cancer
- jejunal neoplasm
- jejunal neuroendocrine tumor G1
- jejunal neuroendocrine tumor, well differentiated, low or intermediate grade
- jejunal somatostatinoma
- joint contractures, osteochondromas, and B-cell lymphoma
- joint laxity, familial
- joint laxity, short stature, and myopia
- jones hersh yusk syndrome
- jugular foramen meningioma
- jugulotympanic paraganglioma
- junctional epidermolysis bullosa
- junctional epidermolysis bullosa Herlitz type
- junctional epidermolysis bullosa inversa
- junctional epidermolysis bullosa with pyloric atresia
- junctional epidermolysis bullosa, non-Herlitz type
- juvenile Huntington disease
- juvenile Paget disease
- juvenile absence epilepsy
- juvenile amyotrophic lateral sclerosis
- juvenile amyotrophic lateral sclerosis with dementia
- juvenile ankylosing spondylitis
- juvenile arthritis due to defect in LACC1
- juvenile breast papillomatosis
- juvenile cataract-microcornea-renal glucosuria syndrome
- juvenile chronic polyarthritis