Disease #06852 (IMD50 (Immunodeficiency 50), OMIM:300988)
Official abbreviation |
IMD50 |
Name |
Immunodeficiency 50 |
OMIM ID |
300988 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MSN |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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