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

3 entries on 1 page. Showing entries 1 - 3.
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00000145 - - - ? ? Saudi Arabia - - - - - SPD - LARP7 LARP7 1 1 Anas M Alazami
00132813 - the CFTR2 database see CFTR2 database for details - - - - - - - - SPD - CFTR CFTR 2 1 Johan den Dunnen
00314627 FamPatV7 PubMed: Landires 2020 - M yes Colombia Indian - - - - SPD see paper; ..., onset pelvic, muscle, 41y-walking with aids, raised CK (4x), contractures elbows, ankles neck and Achilles tendons; inability to climb stairs; not able to stand up from sitting; functional stage VI CAPN3 CAPN3 1 1 Johan den Dunnen
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