 | Prolidase deficiency (PD) is an extremely uncommon autosomal recessive disorder associated with collagen metabolism that affects connective tissues and... 10 KB (1,157 words) - 08:41, 26 July 2023 |
| cause prolidase deficiency. This is characterised by Iminodipeptidurea, skin ulcers, mental retardation and recurrent infections. Serum prolidase falls... 31 KB (3,545 words) - 10:51, 11 April 2024 |
 | types 3, 10 Progeroid and marfanoid aspect-lipodystrophy syndrome Prolidase deficiency Restrictive dermopathy 2 Rienhoff syndrome Ritscher-Schinzel syndrome... 11 KB (1,097 words) - 23:59, 24 March 2024 |
 | Pontocerebellar hypoplasia types 2E, 7, and 12 Potocki-Lupski syndrome Prolidase deficiency Pyknodysostosis RAB23-related Carpenter syndrome Renpenning syndrome... 14 KB (1,343 words) - 23:07, 26 April 2024 |
malonate and acrylonitrile: Hyperprolinemia Inborn error of metabolism Prolidase deficiency Prolinol "Proline". PubChem. U.S. National Library of Medicine. Archived... 23 KB (2,241 words) - 04:41, 26 April 2024 |
 | tarda Primary cutaneous amyloidosis Primary systemic amyloidosis Prolidase deficiency Pseudoporphyria (pseudoporphyria cutanea tarda) Sanfilippo syndrome... 198 KB (17,965 words) - 20:54, 2 May 2024 |
 | autosomal dominant form Oligodendroglioma Peutz–Jeghers syndrome Prolidase deficiency Pseudoachondroplasia Spinocerebellar ataxia type 6 X-linked agammaglobulinemia... 30 KB (2,547 words) - 01:46, 3 December 2023 |
familial Proliferating trichilemmal cyst Prolidase deficiency Prolymphocytic leukemia Properdin deficiency Prosencephaly cerebellar dysgenesis Prosopamnesia... 24 KB (1,908 words) - 03:34, 11 January 2024 |
CYP2C Prolidase deficiency; 170100; PEPD Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome; 225790; FLVCR2 Properdin deficiency, X-linked;... 234 KB (18,877 words) - 15:43, 9 May 2024 |