Disease #00013 (SPD (dwarfism, primordial, syndromic (SPD)))
Official abbreviation |
SPD |
Name |
dwarfism, primordial, syndromic (SPD) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
LARP7 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-07-08 19:59:01 +02:00 (CEST) |
Date last edited |
2015-12-08 23:54:35 +01:00 (CET) |
Individuals
|
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