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

Official abbreviation BCS1
Name cornea, brittle, syndrome, type 1 (BCS-1, corneal fragility keratoglobus, blue sclerae and joint hypermobility)
OMIM ID 229200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ZNF469
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00457301 - PubMed: Skalicka 2024 - M no Czech Republic Czech/Polish - - - - BCS1 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). PRDM1, ZNF469 ZNF469 2 1 Deepak Subramanian
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