Disease #00101 (MMRCS2 (MISMATCH REPAIR CANCER SYNDROME 2), OMIM:619096)

MVZ für Humangenetik Regensburg

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Official abbreviation	MMRCS2
Name	MISMATCH REPAIR CANCER SYNDROME 2
OMIM ID	619096
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MSH2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 09:38:16 +00:00 (UTC)
Date last edited	N/A