Disease #04581 (WNCHRS (Winchester? syndrome (WNCHRS)), OMIM:277950)

Official abbreviation WNCHRS
Name Winchester? syndrome (WNCHRS)
OMIM ID 277950
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MMP14
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Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +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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00154386 22922033-Fam PubMed: Evans 2012, Journal: Evans 2012, PubMed: Winchester 1969 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents (first cousins) F yes Puerto Rico - - - - - WNCHRS severe skeletal/joint deformities, progressive bilateral and symmetric osteolysis carpals and tarsals, interphalangeal joint erosions mimicking rheumatoid arthritis, generalized osteoporosis, eventual loss of function larger joints, including shoulder, elbow, hip, and knee joints; gum hypertrophy, corneal opacities, ECG suggestive myocardial damage MMP14 MMP14 1 2 Johan den Dunnen
00154399 - - - M yes Netherlands - - - - - WNCHRS Mitigated form of Winchester syndrome MMP14 MMP14 1 2 Michel van Geel
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