- autosomal locus
- 常染色体基因座
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal locus
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Autosomal dominant nocturnal frontal lobe epilepsy — (ADNFLE) is a rare epileptic disorder that causes frequent violent seizures during sleep. These seizures often involve complex motor movements, such as hand clenching, arm raising/lowering, and knee bending. Vocalizations such as shouting,… … Wikipedia
Autosomal recessive distal spinal muscular atrophy 1 — Classification and external resources OMIM 604320 Autosomal recessive distal spinal muscular atrophy 1 (or spinal muscular atrophy with respiratory distress type 1, or distal spinal muscular atrophy 1)[1] … Wikipedia
Autosomal-dominante polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp … Deutsch Wikipedia
Autosomal-rezessive polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp … Deutsch Wikipedia
Autosomal dominante polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp … Deutsch Wikipedia
autosomal dominant hypophosphatemic rickets — (ADHR), autosomal dominant vitamin D–resistant rickets a form of familial hypophosphatemic rickets with autosomal dominant inheritance and caused by mutation in the FGF23 gene (locus: 12p13.3), which encodes a member of the fibroblast growth… … Medical dictionary
Silver-Locus — Der Genort Silver Locus (auch: SILV, SI; SIL; ME20; gp100; PMEL17; D12S53E) kodiert ein membranständiges Molekül der Melanosomen (farbstoffproduzierende Organellen) in den pigmentbildenden Zellen (Melanozyten). Dieses Molekül heißt Pmel17 und… … Deutsch Wikipedia
SLC25A4 — Solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4, also known as SLC25A4, is a human gene.cite web | title = Entrez Gene: SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide… … Wikipedia
PEO1 — Chromosome 10 open reading frame 2 Identifiers Symbols C10orf2; ATXN8; FLJ21832; IOSCA; MTDPS7; PEO; PEO1; PEOA3; SANDO; SCA8; TWINL External IDs … Wikipedia
MN gene — The MN blood group in humans is under the control of a pair of co dominant alleles, LMand LN.Most people in the Eskimo population are M/M, while this genotype is rare among Aborigines. In fact, they tend to possess the opposite genotype (N/N).The … Wikipedia
Autoimmune regulator — The Autoimmune Regulator, abbreviated AIRE , is a human gene which is expressed in the thymus. It causes transcription of a wide selection of organ specific genes. This reduces the threat of autoimmunity occurring by allowing the elimination of… … Wikipedia
