Jansen's metaphyseal chondrodysplasia
metaphyseal dysplasia that has material basis in mutation in PTH receptor which results in short-limbed dwarfism
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Jansen's metaphyseal chondrodysplasia
Summary
Jansen's metaphyseal chondrodysplasia is a rare disease[1]. It draws 45 Wikipedia views per month (rare_disease category, ranking #225 of 627).[2]
Key Facts
- Jansen's metaphyseal chondrodysplasia's instance of is recorded as rare disease[3].
- Jansen's metaphyseal chondrodysplasia's instance of is recorded as class of disease[4].
- Jansen's metaphyseal chondrodysplasia is a type of metaphyseal dysplasia[5].
- Jansen's metaphyseal chondrodysplasia is a type of genetic disease[6].
- Jansen's metaphyseal chondrodysplasia is a type of metaphyseal chondrodysplasia[7].
- Jansen's metaphyseal chondrodysplasia is a type of autosomal dominant disease[8].
- Jansen's metaphyseal chondrodysplasia's genetic association is recorded as PTH1R[9].
- Jansen's metaphyseal chondrodysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080020[10].
- Jansen's metaphyseal chondrodysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0080020[11].
- Jansen's metaphyseal chondrodysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- Jansen's metaphyseal chondrodysplasia's has phenotype is recorded as metaphyseal dysplasia[13].
Why It Matters
Jansen's metaphyseal chondrodysplasia draws 45 Wikipedia views per month (rare_disease category, ranking #225 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[14] It is known by 7 alternative names across languages and contexts.[15]