Entry Search - 146510 165240 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '146510 165240 (Search in: MIM number)'
Results: 2 entries.

1:
* 165240. GLI-KRUPPEL FAMILY MEMBER 3; GLI3
Cytogenetic location: 7p14.1, Genomic coordinates (GRCh38): 7:41,960,949-42,264,268
Matching terms: 165240
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
7p14.1 Greig cephalopolysyndactyly syndrome 175700 AD 3
Pallister-Hall syndrome 146510 AD 3
Polydactyly, postaxial, types A1 and B 174200 AD 3
Polydactyly, preaxial, type IV 174700 AD 3
ICD+
SNOMEDCT: 32985001, 56677004, 715707008

2:
# 146510. PALLISTER-HALL SYNDROME; PHS
Cytogenetic location: 7p14.1
Matching terms: 146510
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
7p14.1 Pallister-Hall syndrome 146510 AD 3 GLI3 165240
ICD+
SNOMEDCT: 56677004
ORPHA: 672
DO: 9248
Search: 146510 165240 (Search in: MIM number)
Results: 2 entries.

1:
* 165240. GLI-KRUPPEL FAMILY MEMBER 3; GLI3
Cytogenetic location: 7p14.1, Genomic coordinates (GRCh38): 7:41,960,949-42,264,268
Matching terms: 165240

2:
# 146510. PALLISTER-HALL SYNDROME; PHS
Cytogenetic location: 7p14.1
Matching terms: 146510