Phenotypes for disease #01761 (DKCB1 (dyskeratosis congenita, autosomal recessive, type 1 (DKCB-1)), OMIM:224230)

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AscendingPhenotype ID     

Phenotype details     

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Phenotype/Onset     

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Individual ID     
0000039676 ages diagnosis II2 16y, II3 20y, II5 15y; all reticular skin pigmentation over neck and upper extremities, thickening skin palms/soles; dystrophic changes nails, abnormal dentition (II3, II5 less severe); II2 hypocellular bone marrow with peripheral pancytopenia was only observed; no leukoplakia - - Familial, autosomal recessive - - - - - Johan den Dunnen 00052951
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