Disease #02952 (PPROM (preterm premature rupture of membranes (PPROM)), OMIM:610504)

Official abbreviation PPROM
Name preterm premature rupture of membranes (PPROM)
OMIM ID 610504
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SERPINH1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2016-03-20 12:15:43 +01:00 (CET)


Individuals

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00436589 2637825 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M likely Mexico Hispanic - - - - PPROM Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551 PROM1 PROM1 1 1 Rocio Villafuerte-de la Cruz
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