Chronic kidney disease - OMIM - NCBI

Chronic kidney disease - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

---

• Search OMIM for "Chronic kidney disease " 

1.

#239000 - PAGET DISEASE OF BONE 5, JUVENILE-ONSET; PDB5

Cytogenetic locations: 8q24.12

OMIM:

 

239000

Gene summaries Genetic tests Medical literature

Select item 6038602.

#603860 - MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2

Cytogenetic locations: 16p12.3

OMIM:

 

603860

Gene summaries Genetic tests Medical literature

Select item 1379203.

#137920 - RENAL CYSTS AND DIABETES SYNDROME; RCAD

Cytogenetic locations: 17q12

OMIM:

 

137920

Gene summaries Genetic tests Medical literature

Select item 1739004.

#173900 - POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD1

Cytogenetic locations: 16p13.3

OMIM:

 

173900

Gene summaries Genetic tests Medical literature

Select item 1740005.

#174000 - MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1

Cytogenetic locations: 1q22

OMIM:

 

174000

Gene summaries Genetic tests Medical literature

Select item 5512006.

#551200 - NEPHROPATHY, CHRONIC TUBULOINTERSTITIAL

OMIM:

 

551200

Gene summaries Genetic tests Medical literature

Select item 1203307.

#120330 - PAPILLORENAL SYNDROME; PAPRS

Cytogenetic locations: 10q24.31

OMIM:

 

120330

Gene summaries Genetic tests Medical literature

Select item 2632008.

#263200 - POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD4

HEPATIC FIBROSIS, CONGENITAL, INCLUDED

Cytogenetic locations: 6p12.3-p12.2

OMIM:

 

263200

Gene summaries Genetic tests Medical literature

Select item 3082059.

#308205 - IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME

Cytogenetic locations: Xp22.12

OMIM:

 

308205

Gene summaries Genetic tests Medical literature

Select item 15140010.

#151400 - LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL

OMIM:

 

151400

Gene summaries Genetic tests Medical literature

Select item 60786711.

*607867 - RCC1 DOMAIN- AND BTB DOMAIN-CONTAINING PROTEIN 1; RCBTB1

Cytogenetic locations: 13q14.2

OMIM:

 

607867

Gene summaries Genetic tests Medical literature

Select item 10565012.

#105650 - DIAMOND-BLACKFAN ANEMIA 1; DBA1

Cytogenetic locations: 19q13.2

OMIM:

 

105650

Gene summaries Genetic tests Medical literature

Select item 61764113.

#617641 - CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED

Cytogenetic locations: 1q23.3

OMIM:

 

617641

Gene summaries Genetic tests Medical literature

Select item 16209614.

*162096 - MIDKINE; MDK

Cytogenetic locations: 11p11.2

OMIM:

 

162096

Gene summaries Genetic tests Medical literature

Select item 61309215.

#613092 - HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2

Cytogenetic locations: 1q32.1

OMIM:

 

613092

Gene summaries Genetic tests Medical literature

Select item 60761616.

#607616 - NIEMANN-PICK DISEASE, TYPE B

NIEMANN-PICK DISEASE, TYPE E, INCLUDED

Cytogenetic locations: 11p15.4

OMIM:

 

607616

Gene summaries Genetic tests Medical literature

Select item 26880017.

#268800 - SANDHOFF DISEASE

SANDHOFF DISEASE, ADULT TYPE, INCLUDED

Cytogenetic locations: 5q13.3

OMIM:

 

268800

Gene summaries Genetic tests Medical literature

Select item 22781018.

#227810 - FANCONI-BICKEL SYNDROME; FBS

Cytogenetic locations: 3q26.2

OMIM:

 

227810

Gene summaries Genetic tests Medical literature

Select item 60014219.

#600142 - CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL

Cytogenetic locations: 10q26.13

OMIM:

 

600142

Gene summaries Genetic tests Medical literature

Select item 30150020.

#301500 - FABRY DISEASE

FABRY DISEASE, CARDIAC VARIANT, INCLUDED

Cytogenetic locations: Xq22.1

OMIM:

 

301500

Gene summaries Genetic tests Medical literature