Disease #06622 (MTDPS12A (Mi DNA depletion syndrome 12A (cardiomyopathic type) AD), OMIM:617184)

Official abbreviation MTDPS12A
Name Mi DNA depletion syndrome 12A (cardiomyopathic type) AD
OMIM ID 617184
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SLC25A4
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.