Entry Search - 263200 606702 - OMIM
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Search: '263200 606702 (Search in: MIM number)'
Results: 2 entries.

1:
* 606702. PKHD1 CILIARY IPT DOMAIN-CONTAINING FIBROCYSTIN/POLYDUCTIN; PKHD1
Cytogenetic location: 6p12.3-p12.2, Genomic coordinates (GRCh38): 6:51,615,299-52,087,615
Matching terms: 606702
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
6p12.3-p12.2 Polycystic kidney disease 4, with or without hepatic disease 263200 AR 3
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2:
# 263200. POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD4
HEPATIC FIBROSIS, CONGENITAL, INCLUDED
Cytogenetic location: 6p12.3-p12.2
Matching terms: 263200
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
6p12.3-p12.2 Polycystic kidney disease 4, with or without hepatic disease 263200 AR 3 PKHD1 606702
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ICD+
SNOMEDCT: 28770003
ICD10CM: Q61.1
ICD9CM: 753.14
ORPHA: 731
DO: 0080212
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Search: 263200 606702 (Search in: MIM number)
Results: 2 entries.

1:
* 606702. PKHD1 CILIARY IPT DOMAIN-CONTAINING FIBROCYSTIN/POLYDUCTIN; PKHD1
Cytogenetic location: 6p12.3-p12.2, Genomic coordinates (GRCh38): 6:51,615,299-52,087,615
Matching terms: 606702

2:
# 263200. POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD4
HEPATIC FIBROSIS, CONGENITAL, INCLUDED
Cytogenetic location: 6p12.3-p12.2
Matching terms: 263200


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025