prolidase deficiency

Summary

prolidase deficiency is a developmental defect during embryogenesis^[1]. It draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]

Key Facts

• prolidase deficiency's instance of is recorded as developmental defect during embryogenesis^[3].
• prolidase deficiency's instance of is recorded as rare disease^[4].
• prolidase deficiency's instance of is recorded as class of disease^[5].
• prolidase deficiency's subclass of is recorded as congenital disorder of amino acid metabolism^[6].
• prolidase deficiency's subclass of is recorded as developmental anomaly of metabolic origin^[7].
• prolidase deficiency's subclass of is recorded as syndromic lymphedema^[8].
• prolidase deficiency's subclass of is recorded as genetic syndromic intellectual disability^[9].
• prolidase deficiency's subclass of is recorded as genetic skin vascular disorder^[10].
• prolidase deficiency's subclass of is recorded as neurometabolic disease^[11].
• prolidase deficiency's subclass of is recorded as metabolic skin disease^[12].
• prolidase deficiency's subclass of is recorded as inborn disorder of peptide metabolism^[13].
• prolidase deficiency's subclass of is recorded as amino acid metabolic disorder^[14].
• prolidase deficiency's subclass of is recorded as autosomal recessive disease^[15].
• prolidase deficiency's MeSH descriptor ID is recorded as D056732^[16].
• prolidase deficiency's OMIM ID is recorded as 170100^[17].
• prolidase deficiency's DiseasesDB is recorded as 29838^[18].
• prolidase deficiency's KEGG ID is recorded as H01119^[19].
• prolidase deficiency's MeSH tree code is recorded as C16.131.077.735^[20].
• prolidase deficiency's MeSH tree code is recorded as C16.131.831.720^[21].
• prolidase deficiency's MeSH tree code is recorded as C16.320.565.100.794^[22].
• prolidase deficiency's MeSH tree code is recorded as C16.320.850.746^[23].
• prolidase deficiency's Disease Ontology ID is recorded as DOID:0111540^[24].
• prolidase deficiency's Orphanet ID is recorded as 742^[25].
• prolidase deficiency's NCI Thesaurus ID is recorded as C85029^[26].
• prolidase deficiency's health specialty is recorded as medical genetics^[27].

Why It Matters

prolidase deficiency draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]