Phenotypes for disease #03508 (DKCB2 (dyskeratosis congenita, autosomal recessive, type 2 (DKCB-2)), OMIM:613987)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000039677 nail dystrophy, thrombocytopenia, testicular atrophy, opportunistic infections, growth and mental retardation, liver cirrhosis, intracranial calcification - - Isolated (sporadic) - - - - - Johan den Dunnen 00052952
0000039678 12y-dyskeratosis congenita, mucocutaneous triad of nail dystrophy, leucoplakia, reticulate skin pigmentation; developed peripheral pancytopenia because of progressive bone marrow failure; no other somatic abnormalities reported - - Isolated (sporadic) - - - - - Johan den Dunnen 00052953
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