Additional Disease Briefs

parenteral nutrition-associated cholestasis

Also known as: PNAC

parietal encephalocele

parietal foramina

Also known as: Caitlin marks, catlin marks, enlarged parietal foramina, fenestrae parietales symmetricae, foramina parietalia permagna, hereditary cranium bifidum, parietal foramina, symmetric parietal foramina

parietal foramina 1

Also known as: MSX2 parietal foramina, PFM, PFM1, catlin Marks, cranium bifidum occultum, cranium bifidum, hereditary, foramina parietalia permagna, parietal foramina, parietal foramina 1, parietal foramina caused by mutation in MSX2, parietal foramina, symmetric

parietal foramina 2

Also known as: ALX4 parietal foramina, PFM2, parietal foramina 2, parietal foramina caused by mutation in ALX4, parietal foramina type 2

parietal foramina 3

Also known as: PFM3, parietal foramina 3

parietal foramina with cleidocranial dysplasia

Also known as: PFMCCD, cleidocranial dysplasia with parietal foramina, parietal foramina with clavicular hypoplasia, parietal foramina with cleidocranial dysostosis, parietal foramina with cleidocranial dysplasia

Paris-Trousseau thrombocytopenia

Also known as: Paris-Trousseau syndrome, TCPT, chromosome 11q23 deletion syndrome, thrombocytopenia Paris-Trousseau type, thrombocytopenia, Paris-TROUSSEAU type, thrombocytopenia, Paris-Trousseau type, Isolated cases

Parkinson disease 17

Also known as: PARK17, Parkinson disease 17, Parkinson disease caused by mutation in VPS35, Parkinson disease type 17, Parkinson's disease 17, VPS35 Parkinson disease, autosomal dominant Parkinson disease 17

Parkinson disease 21

Also known as: DNAJC13 hereditary late onset Parkinson disease, PARK21, Parkinson disease 21, Parkinson disease type 21, hereditary late onset Parkinson disease caused by mutation in DNAJC13