Disease #06358 (MGRISCE2 (microcephaly, growth restriction, and increased sister chromatid exchange, type 2), OMIM:618097)

Official abbreviation MGRISCE2
Name microcephaly, growth restriction, and increased sister chromatid exchange, type 2
OMIM ID 618097
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TOP3A
Associated tissues -
Disease features growth restriction, microcephaly, no malar rash, cardiomyopathy, elevated sister chromatid exchanges
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-05-02 19:56:08 +02:00 (CEST)

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