Disease #00573 (PRLMNS (Perlman syndrome (PRLMNS)), OMIM:267000)

Official abbreviation PRLMNS
Name Perlman syndrome (PRLMNS)
OMIM ID 267000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene DIS3L2
Associated tissues -
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Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00117902 - PubMed: Astuti 2012 cell line GM08024 M - - white - 0 - - PRLMNS Wilm tumor DIS3L2 DIS3L2 2 1 Gerard C.P. Schaafsma
00117903 - PubMed: Neri 1984 cell line GM08246 F - - white - 0 - - PRLMNS Wilm tumor DIS3L2 DIS3L2 1 1 Gerard C.P. Schaafsma
00117904 - PubMed: Astuti 2012 died M - Pakistan Pakistani - 0 - - PRLMNS - DIS3L2 DIS3L2 2 1 Gerard C.P. Schaafsma
00117905 - PubMed: Henneveld 1999 died M - Netherlands Dutch - 0 - - PRLMNS - DIS3L2 DIS3L2 1 1 Gerard C.P. Schaafsma
00117906 - PubMed: Henneveld 1999 died F - Netherlands Dutch - 0 - - PRLMNS Wilm tumor DIS3L2 DIS3L2 1 1 Gerard C.P. Schaafsma
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