Disease #01257 (PAPRS (papillorenal syndrome (PAPRS)), OMIM:120330)

Official abbreviation PAPRS
Name papillorenal syndrome (PAPRS)
OMIM ID 120330
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene PAX2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00379776 IR_GH_0135 - - M - Korea, South (Republic) - - - - - PAPRS HP:0030515 HP:0000613 HP:0001123 HP:0000639 HP:0012795 - PAX2 1 1 Jinu Han
00402842 APEC-Patient 5 unpublished familial case F no Mexico - - - - none PAPRS microphthalmia, retinal detachment, optic nerve aplasia. OS: iris coloboma, cataract, optic nerve aplasia, Neurodevelopmental delay, hypotonia, abnormality of the pinna. - PAX2 1 1 Miriam Erandi Reyna-Fabián
00408740 Pat2 Journal: Negrisolo 2023 - M no Italy white - - - - PAPRS bilateral vesicoureteral reflux, chronic renal failure, bilateral renal hypodysplasia, mild hypertrophy bladder neck; ocular and/or ear phenotype PAX2 PAX2 1 1 Susanna Negrisolo
00408741 Pat3/4 Journal: Negrisolo 2023 2 affected twins M no China - - - - - PAPRS renal cystic hypodysplasia, poor growth, developmental delay; one twin cataract, coloboma PAX2 PAX2 1 2 Susanna Negrisolo
00432527 Pat1 Journal: Negrisolo 2023 2-generation family, 1 affected, unaffected non-carrier parents F - Italy - - - - - PAPRS bilateral renal hypodysplasia, vesicoureteral reflux, hearing loss PAX2 PAX2 1 1 Susanna Negrisolo
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