Disease #06289 (DKCA6 (?Dyskeratosis congenita), OMIM:616553)
Official abbreviation |
DKCA6 |
Name |
?Dyskeratosis congenita |
OMIM ID |
616553 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ACD |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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