Kidney Tissue Atlas Ontology
191 terms(s) returned
| Term Type: | Record: 1 to 50 of 191 Records | Page: 1 of 4, First Previous Next Last | Show Records Per Page |
- PEE2
- PEE3
- Pallister-hall syndrome
- Perlman syndrome
- Pierre Robin syndrome associated with a chromosomal anomaly
- Pierson syndrome
- Potter sequence
- Preeyasombat-Varavithya syndrome
- palsy
- pancreas disease
- panuveitis (disease)
- papillary adenocarcinoma
- papillary adenoma
- papillary carcinoma
- papillary epithelial neoplasm
- papillary renal cell carcinoma
- papillary transitional cell carcinoma
- papillary urothelial neoplasm
- papilloma
- paraplegia
- parathyroid gland disease
- paroxysmal nocturnal hemoglobinuria
- paroxysmal nocturnal hemoglobinuria 1
- paroxysmal nocturnal hemoglobinuria 2
- partial autosomal monosomy
- partial autosomal trisomy/tetrasomy
- partial bilateral aplasia of the mullerian ducts
- partial deletion of chromosome 10
- partial deletion of chromosome 11
- partial deletion of chromosome 16
- partial deletion of chromosome 17
- partial deletion of chromosome 2
- partial deletion of chromosome 20
- partial deletion of chromosome 7
- partial deletion of chromosome 8
- partial deletion of chromosome X
- partial deletion of the long arm of chromosome 17
- partial deletion of the long arm of chromosome 22
- partial deletion of the long arm of chromosome 7
- partial deletion of the long arm of chromosome 8
- partial deletion of the long arm of chromosome X
- partial deletion of the short arm of chromosome 10
- partial deletion of the short arm of chromosome 11
- partial deletion of the short arm of chromosome 16
- partial deletion of the short arm of chromosome 2
- partial duplication of chromosome 11
- partial duplication of the short arm of chromosome 11
- partial monosomy of the short arm of chromosome 20
- patellar dysostosis
- patent urachus (disease)
