Entry Search - 600727 613735 - OMIM
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Search: '600727 613735 (Search in: MIM number)'
Results: 2 entries.

1:
* 600727. NUCLEAR FACTOR I/A; NFIA
Cytogenetic location: 1p31.3, Genomic coordinates (GRCh38): 1:61,077,227-61,462,788
Matching terms: 600727
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
1p31.3 Brain malformations with or without urinary tract defects 613735 AD 3

2:
# 613735. BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD
CHROMOSOME 1p32-p31 DELETION SYNDROME, INCLUDED
Cytogenetic location: 1p31.3
Matching terms: 613735
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
1p31.3 Brain malformations with or without urinary tract defects 613735 AD 3 NFIA 600727
ICD+
ORPHA: 401986
DO: 0060409
Search: 600727 613735 (Search in: MIM number)
Results: 2 entries.

1:
* 600727. NUCLEAR FACTOR I/A; NFIA
Cytogenetic location: 1p31.3, Genomic coordinates (GRCh38): 1:61,077,227-61,462,788
Matching terms: 600727

2:
# 613735. BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD
CHROMOSOME 1p32-p31 DELETION SYNDROME, INCLUDED
Cytogenetic location: 1p31.3
Matching terms: 613735