TRIM37 gene related symptoms and diseases
All the information presented here about the TRIM37 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,ORPHANET,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TRIM37 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Very Common - Between 80% and 100% cases |
| Type II diabetes mellitus | Very Common - Between 80% and 100% cases |
| Acanthosis nigricans | Very Common - Between 80% and 100% cases |
| Pointed chin | Very Common - Between 80% and 100% cases |
| Increased body weight | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TRIM37 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Insulin resistance
- Dental crowding
- Epidermal acanthosis
- Pigmentary retinopathy
- Cachexia
- Overgrowth
- Cyanosis
- Growth hormone deficiency
And 65 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to TRIM37 gene
Here you will find a list of rare diseases related to the TRIM37. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MULIBREY NANISM
Alternate names
MULIBREY NANISM Is also known as mulibrey dwarfism, pericardial constriction and growth failure, muscle-liver-brain-eye nanism, perheentupa syndrome, pericardial constriction-growth failure syndrome
Description
MULIBREY nanism (MUL) is a prenatal onset growth disorder with multiorgan manifestations.
Most common symptoms of MULIBREY NANISM
- Intellectual disability
- Short stature
- Generalized hypotonia
- Growth delay
- Hypertelorism
More info about MULIBREY NANISM
Search interest in TRIM37
Potential gene panels for TRIM37 gene
Mulibrey Nanism Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital
This panel specifically test the TRIM37 gene.
More info about this panel United States.
Peroxisomal Disorders Comprehensive NGS Panel Panel
United States.
By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital Peroxisomal Disorders Comprehensive NGS Panel that also includes the following genes: SCP2 ACOX1 CAT PEX26 DNM1L AGPS AGXT GNPAT AMACR HSD17B4
More info about this panel United States.
Comprehensive Primordial Dwarfism Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Comprehensive Primordial Dwarfism Panel that also includes the following genes: PLK4 XRCC4 CRIPT PCNT ORC6 CENPJ CDC6 GMNN RTTN CDK5RAP2
More info about this panel United States.
Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel
Portugal.
By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1
More info about this panel Portugal.
Mulibrey nanism (sequence analysis of TRIM37 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the TRIM37 gene.
More info about this panel Portugal.
Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel
Portugal.
By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1
More info about this panel Portugal.
Mulibrey nanism (sequence analysis of TRIM37 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the TRIM37 gene.
More info about this panel Portugal.
Mulibrey nanism Panel
Poland.
By Laboratory of Genetics BioTe21 Adam Master
This panel specifically test the TRIM37 gene.
More info about this panel Poland.
Mental Retardation and Dysmorphology - panels Panel
Germany.
By MGZ Medical Genetics Center Mental Retardation and Dysmorphology - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panel Germany.
Syndromal Diseases - panels Panel
Germany.
By MGZ Medical Genetics Center Syndromal Diseases - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panel Germany.
Mulibrey nanism Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the TRIM37 gene.
More info about this panel Germany.
Mulibrey nanism Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the TRIM37 gene.
More info about this panel Austria.
Mulibrey nanism Panel
Slovakia.
By MedGene
This panel specifically test the TRIM37 gene.
More info about this panel Slovakia.
Proportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Proportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel that also includes the following genes: ROR2 RPS6KA3 BLM SHOX SHOX2 SMARCAL1 SMC1A SOS1 SOX2 SOX3
More info about this panel United States.
TRIM37 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TRIM37 gene.
More info about this panel United States.
Comprehensive Short Stature Syndrome Panel Panel
Finland.
By Blueprint Genetics Comprehensive Short Stature Syndrome Panel that also includes the following genes: RIT1 BCS1L RRAS SHOX BRAF SMC1A SOS1 SOX2 SOX3 STAT5B
More info about this panel Finland.
3-M Syndrome / Primordial Dwarfism Panel Panel
Finland.
By Blueprint Genetics 3-M Syndrome / Primordial Dwarfism Panel that also includes the following genes: BCS1L XRCC4 PCNT SRCAP ORC6 CENPJ CDC45 CDC6 RTTN CUL7
More info about this panel Finland.
Comprehensive Metabolism Panel Panel
Finland.
By Blueprint Genetics Comprehensive Metabolism Panel that also includes the following genes: BCS1L CNNM2 RYR1 CNNM4 SCN4A SEC23B SGSH SI SLC40A1 SLC12A3
More info about this panel Finland.
Peroxisomal Disorders Panel Panel
Finland.
By Blueprint Genetics Peroxisomal Disorders Panel that also includes the following genes: ACOX1 SUGCT DYM PEX26 EBP AGPS AGXT GNPAT AMACR HSD17B4
More info about this panel Finland.
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Panel
Finland.
By Blueprint Genetics Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel that also includes the following genes: RIT1 RMRP BCS1L ROR2 BGN RRAS RUNX2 BMP1 BMP2 SEC24D
More info about this panel Finland.
Peroxisomal and Lysosomal Diseases , Panel Massive Sequencing (NGS) 78 Genes Panel
Spain.
By Reference Laboratory Genetics Peroxisomal and Lysosomal Diseases , Panel Massive Sequencing (NGS) 78 Genes that also includes the following genes: SCP2 SGSH SLC17A5 SMPD1 ACOX1 MCOLN1 AGXT2 NPC2 CAT DNAJC5
More info about this panel Spain.
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