pseudoachondroplasia
osteochondrodysplasia that has material basis in mutations in the COMP gene which results in short limb dwarfism
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pseudoachondroplasia
Summary
pseudoachondroplasia is a developmental defect during embryogenesis[1]. pseudoachondroplasia draws 65 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #82 of 308).[2]
Key Facts
- pseudoachondroplasia's instance of is recorded as developmental defect during embryogenesis[3].
- pseudoachondroplasia's instance of is recorded as rare disease[4].
- pseudoachondroplasia's instance of is recorded as class of disease[5].
- pseudoachondroplasia's subclass of is recorded as osteochondrodysplasia[6].
- pseudoachondroplasia's subclass of is recorded as multiple epiphyseal dysplasia and pseudoachondroplasia[7].
- pseudoachondroplasia's subclass of is recorded as genetic disease[8].
- pseudoachondroplasia's subclass of is recorded as autosomal dominant disease[9].
- pseudoachondroplasia's subclass of is recorded as dwarfism[10].
- pseudoachondroplasia's Commons category is recorded as Pseudoachondroplasia[11].
- pseudoachondroplasia's MeSH descriptor ID is recorded as C535819[12].
- pseudoachondroplasia's OMIM ID is recorded as 177170[13].
- pseudoachondroplasia's ICD-9 ID is recorded as 756.4[14].
- pseudoachondroplasia's ICD-10 ID is recorded as Q77.3[15].
- pseudoachondroplasia's DiseasesDB is recorded as 32766[16].
- pseudoachondroplasia's KEGG ID is recorded as H00477[17].
- pseudoachondroplasia's GeneReviews ID is recorded as NBK1487[18].
- pseudoachondroplasia's Disease Ontology ID is recorded as DOID:0080047[19].
- pseudoachondroplasia's Orphanet ID is recorded as 750[20].
- pseudoachondroplasia's ICD-9-CM is recorded as 756.9[21].
- pseudoachondroplasia's NCI Thesaurus ID is recorded as C118635[22].
- pseudoachondroplasia's health specialty is recorded as medical genetics[23].
- pseudoachondroplasia's genetic association is recorded as COMP[24].
- pseudoachondroplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080047[25].
- pseudoachondroplasia's exact match is recorded as http://identifiers.org/doid/DOID:0080047[26].
- pseudoachondroplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_750[27].
Why It Matters
pseudoachondroplasia draws 65 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #82 of 308).[2] pseudoachondroplasia has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] pseudoachondroplasia is known by 12 alternative names across languages and contexts.[29]