Disease #05189 (MEHMO;MRXS20;MRXS25 (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (MEHMO)), OMIM:300148)
| Official abbreviation |
MEHMO;MRXS20;MRXS25 |
| Name |
mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (MEHMO) |
| OMIM ID |
300148 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
EIF2S3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-10-06 23:42:30 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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