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Cerulean cataract
6 OMIM references -
4 associated genes
32 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-microcornea syndrome
Nuclear cataract
Zonular cataract
Coppock-like cataract
Cataract with Y-shaped suture opacities
Total congenital cataract
Pulverulent cataract
Coralliform cataract
Posterior polar cataract
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Berardinelli-Seip congenital lipodystrophy
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
46,XX ovotesticular disorder of sex development
46,XX testicular disorder of sex development
Campomelic dysplasia
Acute basophilic leukemia
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Precursor T-cell acute lymphoblastic leukemia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Extraskeletal Ewing sarcoma
Multicentric carpo-tarsal osteolysis with or without nephropathy
Catecholaminergic polymorphic ventricular tachycardia
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Inherited acute myeloid leukemia
Microphthalmia - cataract
Acute promyelocytic leukemia
Synonym(s):
- Blue-dot cataract
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
6 OMIM references -
1 MeSH reference: C537955
Gene symbol UniProt reference OMIM reference
CRYBB2 P43320123620
CRYGD P07320123690
MAF O75444177075
MIP P30301154050
No signs/symptoms info available.