Phenotypes for disease #00621 (STL4 (Stickler syndrome, type IV (STL-4)), OMIM:614134)

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000155493 Congenital sensorineural hyearing loss High myopia Hypoplastic vitreous gel - - Familial, autosomal recessive 06y - - - - Thomas Nixon 00207702
0000155494 Congenital sensorineural hearing loss High myopia Hypoplastic vitreous Flat midface - Stickler Syndrome Familial, autosomal recessive 02y - - - - Thomas Nixon 00207703
0000155495 Congenital sensorineural hearing loss High myopia Hypoplastic vitreous Snailtrack retinal degeneration with round retinal holes Early hip arthropathy - - Familial, autosomal recessive 15y - - - trwn2 Thomas Nixon 00207704
0000155496 Congenital sensorineural hearing loss Myopia Hypoplastic vitreous Mild knee arthropathy - - Familial, autosomal recessive - - - - trwn2 Thomas Nixon 00207705
0000155497 Congenital sensorineural hearing loss High myopia Hypoplastic vitreous gel Severe arthropathy in shoulders and hip Spinal scoliosis - Stickler Syndrome Familial, autosomal recessive 20y - - - - Thomas Nixon 00207706
0000155498 Congenital sensorineural hearing loss High myopia Hypoplastic vitreous - Stickler Syndrome Familial, autosomal recessive 18y - - - - Thomas Nixon 00207707
0000187493 - - - Familial, autosomal recessive - - - - - Julia Lopez 00248524
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.