CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Disease: Cataract microcornea syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.310 GermlineCausalMutation disease ORPHANET Mutational screening of six genes in Chinese patients with congenital cataract and microcornea. 21686328 2011
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.310 GermlineCausalMutation disease ORPHANET [CRYAA gene mutation study in a family with autosomal dominant congenital cataract combined with microcornea]. 21612679 2011
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.310 GermlineCausalMutation disease ORPHANET Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8. 17724170 2007
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		0.310 GeneticVariation disease BEFREE A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family. 16735993 2006