Isodisomy

Isodisomy
Remarkable situation where both chromosomes in a pair are from one parent and neither from the other. Isodisomy causes some birth defects and, we suspect, plays a role in cancer. Also called uniparental disomy.

Medical dictionary. 2011.

Игры ⚽ Нужен реферат?

Look at other dictionaries:

  • Uveal melanoma — Classification and external resources Iris melanoma ICD 10 C69 …   Wikipedia

  • Uniparental disomy — Infobox Disease Name = Uniparental disomy Caption = DiseasesDB = ICD10 = ICD10|Q|99|8|q|90 ICD9 = ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Uniparental disomy (UPD) occurs when a person receives two copies of a… …   Wikipedia

  • Fumarase deficiency — Infobox Disease Name = PAGENAME Caption = Fumarate is converted to malate by fumarase Width = 72px DiseasesDB = 29835 ICD10 = ICD9 = ICDO = OMIM = 606812 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Fumarase deficiency (or fumaric… …   Wikipedia

  • MEST (gene) — Mesoderm specific transcript homolog (mouse), also known as MEST, is a human gene.cite web | title = Entrez Gene: MEST mesoderm specific transcript homolog (mouse)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • USH2A — Usher syndrome 2A (autosomal recessive, mild), also known as USH2A, is a human gene. PBB Summary section title = summary text = This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs …   Wikipedia

  • Laminin, gamma 2 — Laminin, gamma 2, also known as LAMC2, is a human gene.cite web | title = Entrez Gene: LAMC2 laminin, gamma 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=3918| accessdate = ] PBB Summary section title …   Wikipedia

  • RPE65 — Retinal pigment epithelium specific protein 65kDa, also known as RPE65, is a human gene.cite web | title = Entrez Gene: RPE65 retinal pigment epithelium specific protein 65kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

  • MERTK — C mer proto oncogene tyrosine kinase, also known as MERTK, is a human gene.cite web | title = Entrez Gene: MERTK c mer proto oncogene tyrosine kinase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=10461|… …   Wikipedia

  • Cyclic nucleotide gated channel beta 3 — Identifiers Symbols CNGB3; ACHM3 External IDs …   Wikipedia

  • Donnai-Barrow syndrome — Classification and external resources OMIM 222448 Donnai Barrow syndrome is a genetic disorder. It is associated with LRP2.[1] It is an inherited (genetic) disorder that affects many parts of the body …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”