Disease #00013 (SPD (dwarfism, primordial, syndromic (SPD)))

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Official abbreviation	SPD
Name	dwarfism, primordial, syndromic (SPD)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LARP7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-08 19:59:01 +02:00 (CEST)
Date last edited	N/A