Catalog
Cystic or dysplastic kidney disease
No MMS code
Link to WHO Definition
Cystic or dysplastic kidney disease – http://id.who.int/icd/entity/854539401
Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest in other anatomical tissues.
Parents
Children
- Hereditary or congenital cystic or dysplastic kidney disease, inheritance unknown
- Polycystic kidney disease, not elsewhere classified
- Hereditary cystic or dysplastic kidney disease, chromosomal abnormalities
- GB80 Nonfamilial nongenetic cystic kidney disease
- Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys
- Hereditary cystic or dysplastic kidney disease, dominant inheritance
- Senior Boichis syndrome
- Hereditary cystic or dysplastic kidney disease, recessive inheritance
- Renal cystic neoplasms