Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease

1 May 1998

Abstract excerpt

There is a group of inherited cystic nephropathies that are characterized by juvenile onset recessive inheritance (familial juvenile nephronophthisis, FJN) or by adult onset dominant inheritance (medullary cystic disease, MCD) and share similar clinico-pathological presentation to the extent that they are usually grouped together under the term FJN/MCD complex. The main symptoms consist of renal cyst formation in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Kidney Cyst Diseases
Share to Neurogenetic and Muscular Disorders Research
Share to Tissue Engineering and Regenerative Medicine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9536096
DOI: 10.1093/hmg/7.5.905

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney diseasePMID 9536096Read ↗

Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity.Semantic proximity Read ↗

Autosomal-dominant medullary cystic kidney disease type 1: Clinical and molecular findings in six large Cypriot familiesSemantic proximity Read ↗

Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.Semantic proximity Read ↗

Familial Juvenile Hyperuricemic Nephropathy and Autosomal Dominant Medullary Cystic Kidney Disease Type 2Semantic proximity Read ↗

Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41.Semantic proximity Read ↗

Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family.Semantic proximity Read ↗

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31.Semantic proximity Read ↗

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.Semantic proximity Read ↗

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33.Semantic proximity Read ↗

Toward the identification of a gene for familial juvenile nephronophthisis (autosomal recessive medullary cystic kidney disease).Semantic proximity Read ↗

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3Semantic proximity Read ↗

Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.