Phenotypes for disease #00011 (USH3B (Usher syndrome, type 3B (USH-3B)), OMIM:614504)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000002025 lissencephaly, hypoplastic male, agenesis corpus callosum - Familial, X-linked recessive - - - - - - Johan den Dunnen 00003185
0000002097 - - Isolated (sporadic) - - - - - - Johan den Dunnen 00003258
0000301104 retinitis pigmentosa; progressive sensorineural hearing loss; episodic psychosis - Familial, autosomal recessive - Usher syndrome, type 3B (USH-3B) - - - - LOVD 00408986
0000301105 retinitis pigmentosa; progressive sensorineural hearing loss; episodic psychosis - Familial, autosomal recessive - Usher syndrome, type 3B (USH-3B) - - - - LOVD 00408987
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