- USH1C
- Usher syndrome type IC
Medical dictionary. 2011.
USH1C
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USH1C — Usher syndrome 1C (autosomal recessive, severe), also known as USH1C, is a human gene. [cite web | title = Entrez Gene: USH1C Usher syndrome 1C (autosomal recessive, severe)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
USH1C — • Usher syndrome type IC … Dictionary of medical acronyms & abbreviations
Usher syndrome — Classification and external resources OMIM 276900 276901 DiseasesDB 13611 … Wikipedia
Usher 1C — is a human gene. Recessive alleles of this gene are responsible for type 1C Usher syndrome and nonsyndromic deafness.The official name of the gene Usher 1C is “Usher syndrome 1C (autosomal recessive, severe).”USH1C is the gene s official symbol.… … Wikipedia
Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… … Wikipedia
Harmonin — Masse/Länge Primärstruktur 552 Aminosäuren … Deutsch Wikipedia
Usher-Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie H90.3 … Deutsch Wikipedia
Usher Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie … Deutsch Wikipedia
Síndrome de Usher — Clasificación y recursos externos OMIM 276900 … Wikipedia Español
Chromosome 11 (human) — Chromosome 11 Chart Chromosome 11 is one of the 23 pairs of chromosomes in humans. Humans normally have two copies of this chromosome. Chromosome 11 spans about 134.5 million base pairs (the building material of DNA) and represents between 4 and… … Wikipedia
