prolidase deficiency
medical condition
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prolidase deficiency
Summary
prolidase deficiency is a developmental defect during embryogenesis[1].
Key Facts
- prolidase deficiency's instance of is recorded as developmental defect during embryogenesis[2].
- prolidase deficiency's instance of is recorded as rare disease[3].
- prolidase deficiency's instance of is recorded as class of disease[4].
- prolidase deficiency is a type of congenital disorder of amino acid metabolism[5].
- prolidase deficiency is a type of developmental anomaly of metabolic origin[6].
- prolidase deficiency is a type of syndromic lymphedema[7].
- prolidase deficiency is a type of genetic syndromic intellectual disability[8].
- prolidase deficiency is a type of genetic skin vascular disorder[9].
- prolidase deficiency is a type of neurometabolic disease[10].
- prolidase deficiency is a type of metabolic skin disease[11].
- prolidase deficiency is a type of inborn disorder of peptide metabolism[12].
- prolidase deficiency is a type of amino acid metabolic disorder[13].
- prolidase deficiency is a type of autosomal recessive disease[14].
- prolidase deficiency's NCI Thesaurus ID is recorded as C85029[15].
- prolidase deficiency's health specialty is recorded as medical genetics[16].
- prolidase deficiency's genetic association is recorded as PEPD[17].
- prolidase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_742[18].
- prolidase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111540[19].
- prolidase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111540[20].