Please wait while page loads....
Details of LARP7 gene in Homo sapiens
Disease |
|---|
| Disease |
OMIM id |
| Alazami syndrome (ALAZS) [MIM:615071]: A syndromic form of primordial dwarfism, a condition characterized by severe growth restriction that has its onset in utero, and results in short stature and undersize. ALAZS patients manifest severe intellectual disability and distinct facial features including malar hypoplasia, deep-set eyes, broad nose, short philtrum, and macrostomia. Some patients have non-specific and inconsistent skeletal findings, for example, scoliosis and mild epiphyseal changes in the proximal phalanges, but no frank dysplasia. Note=The disease is caused by mutations affecting the gene represented in this entry. |
615071 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Larp7 | CG42569 | --- | Sp-Larp7 |
