LIPH gene related symptoms and diseases
All the information presented here about the LIPH gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to LIPH gene
Symptoms // Phenotype | % Cases |
---|---|
Hyperhidrosis | Very Common - Between 80% and 100% cases |
Palmoplantar hyperkeratosis | Common - Between 50% and 80% cases |
Sparse hair | Common - Between 50% and 80% cases |
Hypotrichosis | Common - Between 50% and 80% cases |
Sparse and thin eyebrow | Common - Between 50% and 80% cases |
Other less frequent symptoms and clinical features
Patients with LIPH gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Sparse eyelashes
- Sparse body hair
- Woolly hair
- Hypotrichosis of the scalp
- Hyperkeratosis
- Brittle hair
Not very common - Between 30% and 50% cases
- Alopecia
- Coarse hair
And 26 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to LIPH gene
Here you will find a list of rare diseases related to the LIPH. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
HYPOTRICHOSIS SIMPLEX
Alternate names
HYPOTRICHOSIS SIMPLEX Is also known as hhs, hereditary hypotrichosis simplex, hts, hypotrichosis simplex, generalized, hereditary
Description
Hypotrichosis simplex (HS) or hereditary hypotrichosis simplex (HHS) is characterized by reduced pilosity over the scalp and body (with sparse, thin, and short hair) in the absence of other anomalies.
Most common symptoms of HYPOTRICHOSIS SIMPLEX
- Alopecia
- Hyperhidrosis
- Sparse hair
- Hypotrichosis
- Sparse and thin eyebrow
More info about HYPOTRICHOSIS SIMPLEX
HYPOTRICHOSIS 7; HYPT7
Alternate names
HYPOTRICHOSIS 7; HYPT7 Is also known as hypotrichosis, localized, autosomal recessive 2, ah, hypotrichosis, total, mari type, hypotrichosis, autosomal recessive, lah2
Most common symptoms of HYPOTRICHOSIS 7; HYPT7
- Hyperhidrosis
- Hyperkeratosis
- Abnormality of the nervous system
- Sparse hair
- Papule
More info about HYPOTRICHOSIS 7; HYPT7
WOOLLY HAIR
Alternate names
WOOLLY HAIR Is also known as wooly hair, familial woolly hair syndrome, hereditary woolly hair syndrome, familial wooly hair syndrome, hereditary wooly hair syndrome
Description
Woolly hair is a rare congenital abnormality of the structure of the scalp hair marked by extreme kinkiness of the hair.
Most common symptoms of WOOLLY HAIR
- Strabismus
- Cataract
- Hyperhidrosis
- Hyperkeratosis
- Nevus
More info about WOOLLY HAIR
Search interest in LIPH
Potential gene panels for LIPH gene
Hypotrichosis (NGS panel of 10 genes) Panel
By CGC Genetics Hypotrichosis (NGS panel of 10 genes) that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelHypotrichosis (NGS panel of 10 genes) Panel
By CGC Genetics Hypotrichosis (NGS panel of 10 genes) that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelHypotrichosis Comprehensive panel Panel
By Connective Tissue Gene Tests Hypotrichosis Comprehensive panel that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelHypotrichosis NGS panel Panel
By Connective Tissue Gene Tests Hypotrichosis NGS panel that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelHypotrichosis Deletion / Duplication panel Panel
By Connective Tissue Gene Tests Hypotrichosis Deletion / Duplication panel that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelHypotrichosis type 7 Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the LIPH gene.
More info about this panelNonsyndromic hypotrichosis panel Panel
By Centogene AG - the Rare Disease Company Nonsyndromic hypotrichosis panel that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 HR
More info about this panelEctodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel Panel
By CeGaT GmbH Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel that also includes the following genes: BCS1L SNRPE SOX18 ST14 TRPS1 IFT122 WNT10A EDARADD SHOC2 LPAR6
More info about this panelPan-Ethnic Carrier Screen: Gene Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Pan-Ethnic Carrier Screen: Gene Sequencing Panel that also includes the following genes: RMRP BCS1L RS1 SACS BLM SGCA SGCB SGCG SGSH SLC12A6
More info about this panelLIPH Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the LIPH gene.
More info about this panelHYPOTRICHOSIS SIMPLEX Panel
By Laboratorio de Genetica Clinica SL HYPOTRICHOSIS SIMPLEX that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 LIPH DSG4 KRT71 KRT74 KRT25
More info about this panelWoolly hair Panel
By Laboratorio de Genetica Clinica SL Woolly hair that also includes the following genes: LPAR6 LIPH KRT71 KRT74 KRT25
More info about this panelWoolly hair/Hypothricosis Simplex: NGS Panel Panel
By Laboratorio de Genetica Clinica SL Woolly hair/Hypothricosis Simplex: NGS Panel that also includes the following genes: RPL21 SNRPE LPAR6 APCDD1 CDSN LIPH DSG4 KRT71 KRT74 KRT25
More info about this panelHypotricosis , Panel Massive Sequencing (NGS) 8 Genes Panel
By Reference Laboratory Genetics Hypotricosis , Panel Massive Sequencing (NGS) 8 Genes that also includes the following genes: RPL21 LPAR6 APCDD1 CDSN LIPH DSG4 KRT74 HR
More info about this panelPan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis Panel
By CEN4GEN Institute for Genomics and Molecular Diagnostics Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis that also includes the following genes: RMRP BCS1L SACS BLM SGCA SGCB SGCG SGSH SLC12A6 SLC17A5
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