Disease #05372 (OZEMA2;OOMD (ocyte/zygote/embryo maturation arrest, type 2), OMIM:616780)

Official abbreviation OZEMA2;OOMD
Name ocyte/zygote/embryo maturation arrest, type 2
OMIM ID 616780
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TUBB8
Associated tissues -
Disease features -
Remarks -
Date created 2017-12-29 16:12:22 +01:00 (CET)
Date last edited 2024-11-08 11:48:51 +01:00 (CET)

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