Entry Search - 116955 602668 - OMIM
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Search: '116955 602668 (Search in: MIM number)'
Results: 2 entries.

1:
* 116955. CCHC-TYPE ZINC FINGER NUCLEIC ACID-BINDING PROTEIN; CNBP
Cytogenetic location: 3q21.3, Genomic coordinates (GRCh38): 3:129,167,827-129,183,896
Matching terms: 116955
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3q21.3 Myotonic dystrophy 2 602668 AD 3
ICD+
SNOMEDCT: 715317001
ICD10CM: G71.11

2:
# 602668. MYOTONIC DYSTROPHY 2; DM2
Cytogenetic location: 3q21.3
Matching terms: 602668
 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
3q21.3 Myotonic dystrophy 2 602668 AD 3 CNBP 116955
Myotonic dystrophy - PS160900 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
3q21.3 Myotonic dystrophy 2 AD 3 602668 CNBP 116955
19q13.32 Myotonic dystrophy 1 AD 3 160900 DMPK 605377
ICD+
SNOMEDCT: 715317001
ICD10CM: G71.11
ORPHA: 606
DO: 0050759
Search: 116955 602668 (Search in: MIM number)
Results: 2 entries.

1:
* 116955. CCHC-TYPE ZINC FINGER NUCLEIC ACID-BINDING PROTEIN; CNBP
Cytogenetic location: 3q21.3, Genomic coordinates (GRCh38): 3:129,167,827-129,183,896
Matching terms: 116955

2:
# 602668. MYOTONIC DYSTROPHY 2; DM2
Cytogenetic location: 3q21.3
Matching terms: 602668