Faster access than browser!Similarities between Chromosome 20 and List of genetic disorders
Chromosome 20 and List of genetic disorders have 8 things in common (in Unionpedia): Alagille syndrome, Chromosome, Endothelin 3, Gene, JAG1, PANK2 (gene), Pantothenate kinase-associated neurodegeneration, Waardenburg syndrome.
Alagille syndrome
Alagille syndrome, Alagille-Watson syndrome or ALGS, is an autosomal dominant genetic disorder that affects the liver, heart, kidney, and other systems of the body.
Alagille syndrome and Chromosome 20 · Alagille syndrome and List of genetic disorders ·
Chromosome
A chromosome (from Ancient Greek: χρωμόσωμα, chromosoma, chroma means colour, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.
Chromosome and Chromosome 20 · Chromosome and List of genetic disorders ·
Endothelin 3
Endothelin-3 is a protein that in humans is encoded by the EDN3 gene.
Chromosome 20 and Endothelin 3 · Endothelin 3 and List of genetic disorders ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Chromosome 20 and Gene · Gene and List of genetic disorders ·
JAG1
Jagged1 (JAG1) is one of five cell surface proteins (ligands) that interact with 4 receptors in the mammalian Notch signaling pathway.
Chromosome 20 and JAG1 · JAG1 and List of genetic disorders ·
PANK2 (gene)
Pantothenate kinase 2, mitochondrial is an enzyme that in humans is encoded by the PANK2 gene.
Chromosome 20 and PANK2 (gene) · List of genetic disorders and PANK2 (gene) ·
Pantothenate kinase-associated neurodegeneration
Pantothenate kinase-associated neurodegeneration (PKAN), also known as neurodegeneration with brain iron accumulation 1 (NBIA1), also called Hallervorden–Spatz syndrome, is a degenerative disease of the brain that can lead to parkinsonism, dystonia, dementia, and ultimately death.
Chromosome 20 and Pantothenate kinase-associated neurodegeneration · List of genetic disorders and Pantothenate kinase-associated neurodegeneration ·
Waardenburg syndrome
Waardenburg syndrome is a rare genetic disorder most often characterized by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation changes.
Chromosome 20 and Waardenburg syndrome · List of genetic disorders and Waardenburg syndrome ·
The list above answers the following questions
- What Chromosome 20 and List of genetic disorders have in common
- What are the similarities between Chromosome 20 and List of genetic disorders
Chromosome 20 and List of genetic disorders Comparison
Chromosome 20 has 123 relations, while List of genetic disorders has 578. As they have in common 8, the Jaccard index is 1.14% = 8 / (123 + 578).
References
This article shows the relationship between Chromosome 20 and List of genetic disorders. To access each article from which the information was extracted, please visit:
