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Diseases

Multicystic Dysplastic Kidney

multicystic dysplastic kidney

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Multicystic Dysplastic Kidney
Standard Disease Name
multicystic dysplastic kidney
MeSH Tree
No data
ICD-10
Q61.4

Identifiers

DO ID
No data
MeSH ID
D021782
OMIM ID
MTHU037030|MTHU036598|MTHU036424
UMLS ID
C3714581
HPO ID
No data

Description and Extensions

Description
NCI2016_NICHD_1602D:Abnormal development of the kidney that is characterized by atretic ureter, multiple cysts of different sizes that are separated by dysplastic parenchyma, and complete lack of function.|NCI2016_02D:Abnormal development of the kidney that is characterized by atretic ureter, multiple cysts of different sizes that are separated by dysplastic parenchyma, and complete lack of function.(NICHD)|MSH2017_2016_08_12:A nongenetic defect due to malformation of the KIDNEY which appears as a bunch of grapes with multiple renal cysts but lacking the normal renal bean shape, and the collection drainage system. This condition can be detected in-utero with ULTRASONOGRAPHY.|HPO2016_07_04:Multicystic dysplasia of the kidney is characterized by multiple cysts of varying size in the kidney and the absence of a normal pelvocaliceal system. The condition is associated with ureteral or ureteropelvic atresia, and the affected kidney is nonfunctional. [HPO:curators]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
06
CPT2
carnitine palmitoyltransferase 2
carnitine palmitoyltransferase 2
07
FLI1
Fli-1 proto-oncogene, ETS transcription factor
Fli-1 proto-oncogene, ETS transcription factor