HYDIN gene related symptoms and diseases
All the information presented here about the HYDIN gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to HYDIN gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Recurrent otitis media | Very Common - Between 80% and 100% cases |
| Ciliary dyskinesia | Very Common - Between 80% and 100% cases |
| Bronchiectasis | Very Common - Between 80% and 100% cases |
| Chronic otitis media | Very Common - Between 80% and 100% cases |
| Nasal polyposis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with HYDIN gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Otitis media
- Dyskinesia
- Cough
- Immotile cilia
- Situs inversus totalis
- Bronchitis
- Recurrent sinusitis
- Pneumonia
And 37 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to HYDIN gene
Here you will find a list of rare diseases related to the HYDIN. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
PRIMARY CILIARY DYSKINESIA
Alternate names
PRIMARY CILIARY DYSKINESIA Is also known as ics, polynesian bronchiectasis, ciliary dyskinesia, primary, 1, with or without situs inversus, pcd, immotile cilia syndrome
Description
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease. Approximately half of PCD patients have an organ laterality defect (situs inversus totalis or situs ambiguus/heterotaxy; see these terms).
Most common symptoms of PRIMARY CILIARY DYSKINESIA
- Hearing impairment
- Ventriculomegaly
- Respiratory distress
- Hydrocephalus
- Headache
More info about PRIMARY CILIARY DYSKINESIA
CILIARY DYSKINESIA, PRIMARY, 5; CILD5
Alternate names
CILIARY DYSKINESIA, PRIMARY, 5; CILD5 Is also known as ciliary dyskinesia, primary, 5, without situs inversus
Description
CILD5 is an autosomal recessive disorder characterized by early onset of a progressive decline in lung function due to an inability to clear mucus and particles from the airways. Affected individuals have recurrent infections of the sinuses, ears, airways, and lungs. Sperm motility is also decreased. Individuals with CILD5 do not have situs inversus (summary by Olbrich et al., 2012).
Most common symptoms of CILIARY DYSKINESIA, PRIMARY, 5; CILD5
- Respiratory insufficiency
- Respiratory distress
- Recurrent infections
- Pneumonia
- Cough
More info about CILIARY DYSKINESIA, PRIMARY, 5; CILD5
Search interest in HYDIN
Potential gene panels for HYDIN gene
Primary Ciliary Dyskinesia Seq + Del/Dup Panel Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Primary Ciliary Dyskinesia Seq + Del/Dup Panel that also includes the following genes: RPGR SPAG1 RSPH1 NME8 LRRC6 INVS CCNO DNAI2 CFTR HYDIN
More info about this panel United States.
Primary Ciliary Dyskinesia Seq Analysis Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Primary Ciliary Dyskinesia Seq Analysis that also includes the following genes: RPGR SPAG1 RSPH1 NME8 LRRC6 INVS CCNO DNAI2 CFTR HYDIN
More info about this panel United States.
Comprehensive Pulmonary-Vascular Seq Analysis Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Comprehensive Pulmonary-Vascular Seq Analysis that also includes the following genes: RPGR BMPR1B BMPR2 SFTPB SLC7A7 SPAG1 TERC TERT NKX2-1 RSPH1
More info about this panel United States.
Comprehensive Pulmonary-Vascular Del/Dup Panel Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Comprehensive Pulmonary-Vascular Del/Dup Panel that also includes the following genes: RPGR BMPR1B BMPR2 SFTPB SLC7A7 SPAG1 TERC TERT NKX2-1 RSPH1
More info about this panel United States.
Primary Ciliary Dyskinesia Del/Dup Panel Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Primary Ciliary Dyskinesia Del/Dup Panel that also includes the following genes: RPGR SPAG1 RSPH1 NME8 LRRC6 INVS CCNO DNAI2 CFTR HYDIN
More info about this panel United States.
Comprehensive Pulmonary-Vascular Seq + Del/Dup Panel Panel
United States.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Comprehensive Pulmonary-Vascular Seq + Del/Dup Panel that also includes the following genes: RPGR BMPR1B BMPR2 SFTPB SLC7A7 SPAG1 TERC TERT NKX2-1 RSPH1
More info about this panel United States.
Ciliary dyskinesia, primary 5 (sequence analysis of HYDIN gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the HYDIN gene.
More info about this panel Portugal.
Ciliopathies (NGS panel for 90 genes) Panel
Portugal.
By CGC Genetics Ciliopathies (NGS panel for 90 genes) that also includes the following genes: SDCCAG8 SPAG1 CEP41 RSPH1 CFAP298 ARL6 NEK8 TMEM237 TRIM32 NME8
More info about this panel Portugal.
Primary ciliary dyskinesia (NGS panel for 27 genes) Panel
Portugal.
By CGC Genetics Primary ciliary dyskinesia (NGS panel for 27 genes) that also includes the following genes: SPAG1 RSPH1 CFAP298 NME8 LRRC6 CCNO DNAI2 HYDIN ZMYND10 DNAAF2
More info about this panel Portugal.
Primary ciliary dyskinesia type 5 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the HYDIN gene.
More info about this panel Germany.
Primary Ciliary Dyskinesia Panel Panel
Germany.
By CeGaT GmbH Primary Ciliary Dyskinesia Panel that also includes the following genes: RPGR SPAG1 RSPH1 CFAP298 NME8 LRRC6 CENPF CCNO DNAI2 HYDIN
More info about this panel Germany.
PRIMARY CILIARY DYSKINESIA Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases PRIMARY CILIARY DYSKINESIA that also includes the following genes: NME8 LRRC6 DNAI2 HYDIN RSPH9 RSPH4A DNAL1 CCDC39 DNAAF5 CCDC40
More info about this panel Spain.
HYDIN Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the HYDIN gene.
More info about this panel United States.
Primary Ciliary Dyskinesia Panel Panel
Finland.
By Blueprint Genetics Primary Ciliary Dyskinesia Panel that also includes the following genes: RPGR SPAG1 RSPH1 CFAP298 NME8 LRRC6 INVS CENPF CCNO DNAI2
More info about this panel Finland.
Complement System Disorder Panel Panel
Finland.
By Blueprint Genetics Complement System Disorder Panel that also includes the following genes: CFB SPAG1 THBD SERPING1 RSPH1 C1QA C1QB C1QBP C1QC C1S
More info about this panel Finland.
CILIARY DYSKINESIA, PRIMARY NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL CILIARY DYSKINESIA, PRIMARY NGS PANEL that also includes the following genes: SPAG1 RSPH1 CFAP298 NME8 LRRC6 CCNO DNAI2 HYDIN ZMYND10 DNAAF2
More info about this panel Spain.
Primary Ciliary Dyskinesia , Panel Massive Sequencing (NGS) 17 Genes Panel
Spain.
By Reference Laboratory Genetics Primary Ciliary Dyskinesia , Panel Massive Sequencing (NGS) 17 Genes that also includes the following genes: NME8 LRRC6 DNAI2 HYDIN RSPH9 RSPH4A DNAL1 CCDC39 DNAAF5 CCDC40
More info about this panel Spain.
Primary Ciliary Dyskinesia: gene sequencing panel Panel
Canada.
By CEN4GEN Institute for Genomics and Molecular Diagnostics Primary Ciliary Dyskinesia: gene sequencing panel that also includes the following genes: SPAG1 RSPH1 CFAP298 NME8 LRRC6 CCNO DNAI2 HYDIN ZMYND10 DNAAF2
More info about this panel Canada.
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