Disease #05348 (MIMIS (microcephaly-micromelia syndrome (MIMIS)), OMIM:251230)
| Official abbreviation |
MIMIS |
| Name |
microcephaly-micromelia syndrome (MIMIS) |
| OMIM ID |
251230 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DONSON |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
autosomal recessive |
| Date created |
2017-11-17 14:47:27 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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