Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Autosomal recessive nonsyndromic hearing loss 12
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the CDH23 gene on chromosome 10q22. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 39
An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor. It is characterized by profound deafness. [from NCI]
Autosomal recessive nonsyndromic hearing loss 49
Autosomal recessive deafness-49 (DFNB49) is characterized by prelingual profound sensorineural hearing loss at all frequencies (Riazuddin et al., 2006 and Chishti et al., 2008). [from OMIM]
Autosomal recessive nonsyndromic hearing loss 15
This form of autosomal recessive deafness is sensorineural and nonsyndromic, and shows prelingual onset (summary by Charizopoulou et al., 2011). [from OMIM]
Autosomal recessive nonsyndromic hearing loss 44
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ADCY1 gene. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 85
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 17p12-q11.2. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 45
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 1q43-q44. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 104
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the RIPOR2 gene. [from MONDO]
Usher syndrome, type 1M
Usher syndrome type 1M (USH1M) is characterized by prelingual sensorineural hearing loss, vestibular dysfunction, and retinitis pigmentosa (Ahmed et al., 2018). For a general phenotypic description and discussion of genetic heterogeneity of Usher syndrome, see USH1 (276900). [from OMIM]
Autosomal recessive nonsyndromic hearing loss 83
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 9p23-p21.2. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 71
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 8p22-p21.3. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 62
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 12p13.2-p11.23. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 40
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 38
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 6q26-q27. [from MONDO]
Prelingual sensorineural hearing impairment
A form of sensorineural deafness with either congenital onset or infantile onset, i.e., before the acquisition of speech. [from HPO]
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on