Disease #03510 (DKCA2;DCKB4 (dyskeratosis congenita, autosomal dominant, type 2 (DKCA-2, autosomal recessive (DKCB-4))), OMIM:613989)
Official abbreviation |
DKCA2;DCKB4 |
Name |
dyskeratosis congenita, autosomal dominant, type 2 (DKCA-2, autosomal recessive (DKCB-4)) |
OMIM ID |
613989 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
14 |
Phenotype entries for this disease |
14 |
Associated with 1 gene |
TERT |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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