rs104894049
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
0.810
GeneticVariation
BEFREE
Missense mutation in the SHH gene (I111F ) at 7q36 may be associated with SMMCI .
16722608
2006
rs104894049
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
0.810
GeneticVariation
UNIPROT
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.
15103725
2004
rs104894049
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
0.810
GeneticVariation
UNIPROT
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.
11471164
2001
rs104894049
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
A
0.810
CausalMutation
CLINVAR
rs104894040
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs104894042
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs104894043
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs104894048
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs104894050
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs267607047
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
19603532
2009
rs104894040
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs104894042
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs104894043
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs104894048
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs104894050
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs267607047
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
17001669
2006
rs104894040
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Molecular mechanisms of Sonic hedgehog mutant effects in holoprosencephaly.
16282375
2005
rs104894040
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
SHH Ile111Asp in alobar holoprosencephaly in a proposita, whose mother had only a solitary median maxillary incisor.
15942952
2005
rs104894040
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation.
15942953
2005
rs104894042
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Molecular mechanisms of Sonic hedgehog mutant effects in holoprosencephaly.
16282375
2005
rs104894042
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation.
15942953
2005
rs104894042
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
SHH Ile111Asp in alobar holoprosencephaly in a proposita, whose mother had only a solitary median maxillary incisor.
15942952
2005
rs104894043
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Molecular mechanisms of Sonic hedgehog mutant effects in holoprosencephaly.
16282375
2005
rs104894043
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
SHH Ile111Asp in alobar holoprosencephaly in a proposita, whose mother had only a solitary median maxillary incisor.
15942952
2005
rs104894043
×
Entrez Id:
6469
Gene Symbol:
SHH
SHH
HOLOPROSENCEPHALY 3
0.800
GeneticVariation
UNIPROT
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation.
15942953
2005