Phenotypes for disease #03509 (DKCB3 (dyskeratosis congenita, autosomal recessive, type 3 (DKCB-3)), OMIM:613988)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000039679 oral leukoplakia, nail dystrophy, abnormal skin pigmentation, bone marrow failure, developed squamous cell carcinoma of the tongue; telomere lengths <1 percentile - - Isolated (sporadic) - - - - - Johan den Dunnen 00052954
0000039680 oral leukoplakia, nail dystrophy, abnormal skin pigmentation, bone marrow failure; telomere lengths <1 percentile - - Isolated (sporadic) - - - - - Johan den Dunnen 00052955
0000060556 Dyskeratosis congenita, autosomal recessive 4 (OMIM:613989) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080987
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