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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