Disease #02022 (PKD4 (kidney, polycystic, disease, type 4, with/without hepatic disease (PKD4)), OMIM:263200)

Official abbreviation PKD4
Name kidney, polycystic, disease, type 4, with/without hepatic disease (PKD4)
OMIM ID 263200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 7
Associated with 1 gene PKHD1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-05-29 16:02:08 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00080834 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - PKD4 Polycystic kidney and hepatic disease (OMIM:263200) PKHD1 PKHD1 1 1 Daniel Trujillano
00275525 SAYER - - F ? Oman - >04y - - - PKD4 Hypertension CKD Congenital hepatic fibrosis PKHD1 PKHD1 2 1 John Sayer
00275526 SAYER - - M yes Oman - >00y01m - - - PKD4 Hypertension CKD Congestive heart failure PKHD1 PKHD1 1 1 John Sayer
00275527 SAYER - - M yes Oman - >00y01m - - - PKD4 Hypertension Congenital hepatic fibrosis PKHD1 PKHD1 1 1 John Sayer
00314937 - - Fetal, Second Trimester ? no China Asian - - - - PKD4 oligohydramnios (HP:0001562), abnormality intrahepatic bile duct (HP:0011040), enlarged kidney (HP:0000105), polycystic kidney dysplasia (HP:0000113), congenital hepatic fibrosis (HP:0002612) PKHD1 PKHD1 2 1 Zhao SZ
00314957 - - fetal,second trimester ? no China Asian - - - - PKD4 oligohydramnios (HP:0001562),enlarged kidney (HP:0000105) PKHD1 PKHD1 3 1 Zhao SZ
00436423 - - 2-generation family, 1 affected (M), unaffected heterozygous carrier parents F no China Chinese >07y - yes Liver transplantation PKD4 - PKHD1 PKHD1 3 1 Chen Qian
00466658 family - - F yes Oman - 00y00m - - - PKD4 Multiple congenital anomalies, bilateral palpable kidney masses, dysmorphic features. PKHD1 PKHD1 1 1 John Sayer
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