Disease #00551 (STL2 (Stickler syndrome, type II (STL-2)), OMIM:604841)

Official abbreviation STL2
Name Stickler syndrome, type II (STL-2)
OMIM ID 604841
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene COL11A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00238991 - - - F no - - - - - - STL2 - COL11A1, COL11A2, COL2A1, COL9A1, COL9A2, COL9A3 COL11A1 2 1 Allan Richards
00324654 173550 - - M ? Germany - - - - - STL2 high myopia; hearing loss COL11A1 COL11A1 1 1 Andreas Laner
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