Disease #02738 (TNZD (zinc deficiency, transient neonatal (incl. breast milk, TNZD)), OMIM:608118)
Official abbreviation |
TNZD |
Name |
zinc deficiency, transient neonatal (incl. breast milk, TNZD) |
OMIM ID |
608118 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC30A2 |
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) |
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