Display Settings:

Format
Items per page

Send to:

Choose Destination

Results: 11

1.

Wilms tumor 1

MedGen UID:
447509
Concept ID:
CN033288
Disease or Syndrome
2.

Hyperploidy

A chromosomal abnormality in that is characterized by an addition of chromosomes that results in a chromosome number that is not an exact multiple of the haploid number. [from NCI]

MedGen UID:
266278
Concept ID:
C1305143
Cell or Molecular Dysfunction
3.

Cystic Partially Differentiated Nephroblastoma

A variant of Wilm tumor of the kidney characterized by the presence of cystic spaces separated by septa. The septa contain immature epithelial cells, immature stromal cells, and blastema cells. Surgical resection is usually curative. [from NCI]

MedGen UID:
220423
Concept ID:
C1266139
Neoplastic Process
4.

Trisomy 12

A chromosomal abnormality consisting of the presence of a third copy of chromosome 12 in somatic cells. [from NCI]

MedGen UID:
98492
Concept ID:
C0432408
Disease or Syndrome
5.

Cystic disease of kidney

A congenital or acquired kidney disorder characterized by the presence of renal cysts. [from NCI]

MedGen UID:
352142
Concept ID:
C1691228
Disease or Syndrome
6.

Male Urogenital Diseases

Pathological processes of the male URINARY TRACT and the reproductive system (GENITALIA, MALE). [from MeSH]

MedGen UID:
318601
Concept ID:
C1720894
Disease or Syndrome
7.

Female Urogenital Diseases

Pathological processes of the female URINARY TRACT and the reproductive system (GENITALIA, FEMALE). [from MeSH]

MedGen UID:
318599
Concept ID:
C1720887
Disease or Syndrome
8.

Female Urogenital Diseases and Pregnancy Complications

Pathological processes of the female URINARY TRACT, the reproductive system (GENITALIA, FEMALE), and disorders related to PREGNANCY. [from MeSH]

MedGen UID:
318565
Concept ID:
C1720765
Disease or Syndrome
9.

Duplication of chromosome

An aberration in which an extra chromosome or a chromosomal segment is made. [from MeSH]

MedGen UID:
275730
Concept ID:
C1516516
Cell or Molecular Dysfunction
10.

Genetic Diseases, Inborn

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from MeSH]

MedGen UID:
181981
Concept ID:
C0950123
Disease or Syndrome
11.

Aneuploidy

The chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1). [from MeSH]

MedGen UID:
294
Concept ID:
C0002938
Cell or Molecular Dysfunction

Display Settings:

Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...