Entry Search - 164005 614753 - OMIM
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Search: '164005 614753 (Search in: MIM number)'
Results: 2 entries.

1:
* 164005. NUCLEAR FACTOR I/X; NFIX
Cytogenetic location: 19p13.13, Genomic coordinates (GRCh38): 19:12,995,475-13,098,796
Matching terms: 164005
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
19p13.13 Malan syndrome 614753 AD 3
Marshall-Smith syndrome 602535 AD 3
ICD+
SNOMEDCT: 73284007, 763795006

2:
# 614753. MALAN SYNDROME; MALNS
Cytogenetic location: 19p13.13
Matching terms: 614753
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
19p13.13 Malan syndrome 614753 AD 3 NFIX 164005
ICD+
SNOMEDCT: 763795006
ORPHA: 420179
DO: 0112102
Search: 164005 614753 (Search in: MIM number)
Results: 2 entries.

1:
* 164005. NUCLEAR FACTOR I/X; NFIX
Cytogenetic location: 19p13.13, Genomic coordinates (GRCh38): 19:12,995,475-13,098,796
Matching terms: 164005

2:
# 614753. MALAN SYNDROME; MALNS
Cytogenetic location: 19p13.13
Matching terms: 614753