GeneSet Information

Tier II GS234130 • [MeSH] Genetic Diseases, Inborn : D030342

DESCRIPTION:

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. Generated by gene2mesh v. 1.1.1

LABEL:

Genetic Diseases, Inborn

SCORE TYPE:

Binary

DATE ADDED:

2015-09-11

DATE UPDATED:

2024-04-25

SPECIES:

No publication information is associated with this GeneSet.

Annotation Information

No sequence read archive data associated with this GeneSet.


No annotations are associated with this GeneSet.

Gene List • 2800 Genes

Uploaded As Gene Symbol Homology Score Priority LinkOuts Emphasis