chondrodysplasia punctata

Summary

chondrodysplasia punctata is a developmental defect during embryogenesis^[1]. It draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).^[2]

Key Facts

• chondrodysplasia punctata's instance of is recorded as developmental defect during embryogenesis^[3].
• chondrodysplasia punctata's instance of is recorded as class of disease^[4].
• chondrodysplasia punctata is a type of primary bone dysplasia^[5].
• chondrodysplasia punctata is a type of syndrome^[6].
• chondrodysplasia punctata is a type of genetic disease^[7].
• chondrodysplasia punctata is a type of monogenic disease^[8].
• chondrodysplasia punctata's symptoms and signs is recorded as stippled epiphyses^[9].
• chondrodysplasia punctata's ICD-9-CM is recorded as 756.59^[10].
• chondrodysplasia punctata's NCI Thesaurus ID is recorded as C84632^[11].
• chondrodysplasia punctata's health specialty is recorded as medical genetics^[12].
• chondrodysplasia punctata's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2581^[13].
• chondrodysplasia punctata's exact match is recorded as http://identifiers.org/doid/DOID:2581^[14].
• chondrodysplasia punctata's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93442^[15].
• chondrodysplasia punctata's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].

Why It Matters

chondrodysplasia punctata draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).^[2]