Mental Retardation, X-Linked
|
0.520 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
|
23871722 |
2013 |
Mental Retardation, X-Linked
|
0.520 |
Biomarker
|
disease |
BEFREE |
ZNF674 belongs to a cluster of seven highly related zinc-finger genes in Xp11, two of which (ZNF41 and ZNF81) were implicated previously in XLMR.
|
16385466 |
2006 |
Mental Retardation, X-Linked
|
0.520 |
GeneticVariation
|
disease |
BEFREE |
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
|
14628291 |
2003 |
Mental Retardation, X-Linked
|
0.520 |
Biomarker
|
disease |
CTD_human |
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
|
14628291 |
2003 |
Mental Retardation, X-Linked 1
|
0.310 |
GeneticVariation
|
disease |
ORPHANET |
XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
|
23871722 |
2013 |
Mental Retardation, X-Linked 1
|
0.310 |
GeneticVariation
|
disease |
BEFREE |
Moreover, screening of a panel of patients with MRX led to the identification of two other ZNF41 mutations that were not found in healthy control individuals.
|
14628291 |
2003 |
MENTAL RETARDATION, X-LINKED 89
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
|
23871722 |
2013 |
Cognition Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
|
14628291 |
2003 |
Drooling
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Facial paralysis
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Flatfoot
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Meckel Diverticulum
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Moderate intellectual disability
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Obesity
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Pyloric Stenosis
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Babinski Reflex
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Severe intellectual disability
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Urinary Incontinence
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Macrocephaly
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Small for gestational age (disorder)
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Late tooth eruption
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Small for gestational age fetus
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Downward slant of palpebral fissure
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Broad nasal tip
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Delayed speech and language development
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|