Gene USH1C function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
USH1C	Usher syndrome 1C (autosomal recessive, severe)	HGNC:2824, PDZ73, harmonin, NY-CO-37, NY-CO-38, PDZ-73/NY-CO-38, AIE-75	deafness, autosomal recessive 18

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MeSH term

Frequency	Condition_Probility
Adolescent	2	0.0
Female	5	0.0
Hearing Loss, Sensorineural/*genetics	3	3.0
Humans	14	0.0
Male	5	0.0
Mutation/*genetics	2	0.0
Pedigree	6	0.0
Polymorphism, Single-Stranded Conformational	3	0.0
Research Support, Non-U.S. Gov't	11	0.0
Retinitis Pigmentosa/*genetics	3	2.0
Syndrome	10	0.0
Animals	5	0.0
Alleles	3	0.0
Linkage (Genetics)	4	0.0
Mice	4	0.0
Microsatellite Repeats	3	0.0
Research Support, U.S. Gov't, P.H.S.	10	0.0
Base Sequence	2	0.0
DNA Mutational Analysis	3	0.0
Molecular Sequence Data	2	0.0
*Mutation	2	0.0
Protein Isoforms	2	0.0
Retinal Degeneration/*genetics	2	5.0
Transcription, Genetic	2	0.0
Chromosome Mapping	6	0.0
*Chromosome Mapping	2	0.0
*Chromosomes, Human, Pair 11	5	0.0
Deafness/*genetics	3	2.0
Genes, Recessive	4	0.0
Haplotypes	4	0.0
Lod Score	2	0.0
Bacteriophage P1/genetics	2	8.0
Canada/ethnology	2	22.0
Chromosomes, Artificial, Yeast	2	0.0
Cloning, Molecular	2	0.0
France/ethnology	2	5.0
Louisiana/epidemiology	2	22.0
Sequence Analysis, DNA	2	0.0
Chromosomes, Human, Pair 11/*genetics	2	0.0
DNA Primers/chemistry	2	0.0
Louisiana	2	10.0
Genetic Markers	2	0.0
Quebec/ethnology	2	66.0
Carrier Proteins/*genetics	3	0.0