Phenotypes for disease #01792 (BCS1 (cornea, brittle, syndrome, type 1 (BCS-1, corneal fragility keratoglobus, blue sclerae and joint hypermobility)), OMIM:229200)

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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     
0000345775 Myopia (HP:0000545); decreased corneal thickness (HP:0100689); corneal stromal edema (HP:0012040); blue sclerae (HP:0000592); abnormal scleral thickness (HP:6000841 ); reduced visual acuity (HP:0007663); corneal rupture (HP:0100583); ectopia lentis (HP:0001083); ectopia lentis (HP:0001083 ); retinal detachment (HP:0000541); childhood onset sensorineural hearing impairment (HP:0011474); mitral regurgitation (HP:0001653); tricuspid regurgitation (HP:0005180); incomplete right bundle branch block (HP:6000313); kyphoscoliosis (HP:0002751); clinodactyly (HP:0030084); hallux valgus (HP:0001822); inguinal hernia (HP:0000023); carious teeth (HP:0000670). Stickler syndrome BCS1 Familial, autosomal recessive 26y 40y 03y Myopia (HP:0000545) - Deepak Subramanian 00457301
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