Disease #02915 (CTCRT-21;CCA-4 (cataract, type 21, multiple types (CTRCT-21, cataract, cerulean, congenital, type 4 (CCA-4))), OMIM:610202)

Official abbreviation CTCRT-21;CCA-4
Name cataract, type 21, multiple types (CTRCT-21, cataract, cerulean, congenital, type 4 (CCA-4))
OMIM ID 610202
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MAF
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Disease features -
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Individuals

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00382147 96 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - 0 - - CTCRT-21;CCA-4 congenital cataract; MIM, 610202 MAF MAF 1 1 LOVD
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