Entry Search - 102579 614575 - OMIM
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Search: '102579 614575 (Search in: MIM number)'
Results: 2 entries.

1:
* 102579. REPLICATION FACTOR C, SUBUNIT 1; RFC1
Cytogenetic location: 4p14, Genomic coordinates (GRCh38): 4:39,287,456-39,366,362
Matching terms: 102579
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
4p14 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 614575 AR 3
ICD+
SNOMEDCT: 1236804009

2:
# 614575. CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS
Cytogenetic location: 4p14
Matching terms: 614575
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
4p14 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 614575 AR 3 RFC1 102579
ICD+
SNOMEDCT: 1236804009
ORPHA: 504476
Search: 102579 614575 (Search in: MIM number)
Results: 2 entries.

1:
* 102579. REPLICATION FACTOR C, SUBUNIT 1; RFC1
Cytogenetic location: 4p14, Genomic coordinates (GRCh38): 4:39,287,456-39,366,362
Matching terms: 102579

2:
# 614575. CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS
Cytogenetic location: 4p14
Matching terms: 614575