Phenotypes for disease #04581 (WNCHRS (Winchester? syndrome (WNCHRS)), OMIM:277950)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000127063 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 - - Familial, autosomal recessive - - - - - Johan den Dunnen 00154386
0000127074 Mitigated form of Winchester syndrome - - Familial, autosomal recessive - - - - - Michel van Geel 00154399
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