Phenotypes for disease #03893 (PRLTS4 (Perrault syndrome, type 4 (PRLTS4)), OMIM:615300)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000043002 see paper; ... - - Familial, autosomal recessive - - - - - Leigh Demain 00056383
0000043003 see paper; ... - - Familial, autosomal recessive - - - - - Leigh Demain 00056384
0000223435 sensorineural hearing loss (HP:0000407),premature ovarian insufficiency (HP:0008209) - Perrault syndrome, type 4 (PRLTS-4) Familial, autosomal recessive 24y - - - - Zhaoyu Pan 00295959
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