Phenotypes for disease #00115 (CRMCC (microangiopathy, cerebroretinal, with calcifications and cysts (CRMCC, Coats plus syndrome)), OMIM:612199)

32 entries on 1 page. Showing entries 1 - 32.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000000060 - Familial, autosomal recessive 15y - - - - - - LOVD 00000371
0000000061 - Familial, autosomal recessive 24y - - - - - - LOVD 00000372
0000000062 - Familial, autosomal recessive 20y - - - - - - LOVD 00000373
0000000063 - Familial, autosomal recessive 25y - - - - - - LOVD 00000374
0000000064 - Familial, autosomal recessive 22y - - - - - - LOVD 00000375
0000000065 - Familial, autosomal recessive 28y - - - - - - LOVD 00000376
0000000066 - Familial, autosomal recessive 22y - - - - - - LOVD 00000377
0000000067 - Familial, autosomal recessive 13y - - - - - - LOVD 00000378
0000000068 - Familial, autosomal recessive 18y - - - - - - LOVD 00000379
0000000069 - Familial, autosomal recessive 02y - - - - - - LOVD 00000380
0000000071 - Familial, autosomal recessive 03y - - - - - - LOVD 00000382
0000000072 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000383
0000000073 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000384
0000000074 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000385
0000000075 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000386
0000000076 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000387
0000000077 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000388
0000000078 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000389
0000000079 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000390
0000000080 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000391
0000000081 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000392
0000000082 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000393
0000000083 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000394
0000000084 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000396
0000000094 - Familial, autosomal recessive - - - - - - - Anne Polvi 00000404
0000027974 - Familial, autosomal recessive 02y10m - - - - - - Anne Polvi 00034569
0000028090 - Familial, autosomal recessive 16y - - 03y - - - Anne Polvi 00037569
0000028316 - Familial, autosomal recessive - - - - - Coats plus syndrome; dextrocardia, situs inversus; see paper ... - Anne Polvi 00037771
0000061061 - Familial, autosomal recessive - - - - - intrauterine growth retardation, intracranial calcification in a distribution typical of CP, leukoencephalopathy, retinal exudates typical of CP; sparse hair (1), 3y-fractures (1), 3y-GI ectasias (1) - Johan den Dunnen 00081459
0000061385 - Familial, autosomal recessive - - - - - - - Anne Polvi 00081744
0000061386 - Familial, autosomal recessive - - - - - - - Anne Polvi 00081745
0000127133 CRMCC Unknown 00y08m CRMCC 00y08m 00y 00y - - Anne Polvi 00154407
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