multiple epiphyseal dysplasia
osteochondrodysplasia that has material basis in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain
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multiple epiphyseal dysplasia
Summary
multiple epiphyseal dysplasia is a rare disease[1]. It ranks in the top 0.32% of rare_disease entities by monthly Wikipedia readership (491 views/month, #2 of 627).[2]
Key Facts
- multiple epiphyseal dysplasia's instance of is recorded as rare disease[3].
- multiple epiphyseal dysplasia's instance of is recorded as class of disease[4].
- multiple epiphyseal dysplasia is a type of osteochondrodysplasia[5].
- multiple epiphyseal dysplasia is a type of developmental defect during embryogenesis[6].
- multiple epiphyseal dysplasia is a type of genetic disease[7].
- multiple epiphyseal dysplasia's Commons category is recorded as Multiple epiphyseal dysplasia[8].
- multiple epiphyseal dysplasia's symptoms and signs is recorded as arthralgia[9].
- multiple epiphyseal dysplasia's ICD-9-CM is recorded as 756.56[10].
- multiple epiphyseal dysplasia's health specialty is recorded as medical genetics[11].
- multiple epiphyseal dysplasia's genetic association is recorded as COL9A2[12].
- multiple epiphyseal dysplasia's genetic association is recorded as COL9A3[13].
- multiple epiphyseal dysplasia's genetic association is recorded as COL9A1[14].
- multiple epiphyseal dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12721[15].
- multiple epiphyseal dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:12721[16].
- multiple epiphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_166002[17].
- multiple epiphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_251[18].
- multiple epiphyseal dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
multiple epiphyseal dysplasia ranks in the top 0.32% of rare_disease entities by monthly Wikipedia readership (491 views/month, #2 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[20] It is known by 14 alternative names across languages and contexts.[21]