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
|