nonsyndromic
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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
nonsyndromic — non·syn·drom·ic (non″sin dromґik) not occurring as part of a syndrome … Medical dictionary
Craniosynostosis — Classification and external resources Child with premature closure (craniosynostosis) of the lambdoid suture. Notice the swelling on the right side of the head ICD 10 … Wikipedia
Hearing impairment — See also: Deaf culture for the social movement.. Deaf and/or hard of hearing Classification and external resources The International Symbol for Deafness … Wikipedia
TECTA — Tectorin alpha, also known as TECTA, is a human gene.cite web | title = Entrez Gene: TECTA tectorin alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7007| accessdate = ] PBB Summary section title =… … Wikipedia
OTOF — Otoferlin Identifiers Symbols OTOF; AUNB1; DFNB6; DFNB9; FER1L2; NSRD9 External IDs … Wikipedia
GJB6 — Gap junction protein, beta 6, 30kDa Identifiers Symbols GJB6; CX30; DFNA3; DFNA3B; DFNB1B; ED2; EDH; HED External IDs … Wikipedia
Wolfram syndrome — Classification and external resources Photographic image of the patient right eye showing optic atrophy without diabetic ret … Wikipedia
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
CDH23 — Cadherin like 23, also known as CDH23, is a human gene. PBB Summary section title = summary text = This gene is a member of the cadherin superfamily, genes encoding calcium dependent cell cell adhesion glycoproteins. The protein encoded by this… … Wikipedia
