Hypotrichosis 13; Hypt13

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Hypotrichosis 13; Hypt13

KRT71

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Hypotrichosis 13; Hypt13

Hyperhidrosis
Sparse hair
Papule
Hypotrichosis
Sparse and thin eyebrow
Woolly hair

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Hypotrichosis 13; Hypt13 Is also known as hypotrichosis with woolly hair.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Hypotrichosis 13; Hypt13 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Hypotrichosis 13 (sequence analysis of KRT71 gene). By CGC Genetics (Portugal). KRT71 Specificity 100 % Genes 100 %
Hypotrichosis (NGS panel of 10 genes). By CGC Genetics (Portugal). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Hypotrichosis (NGS panel of 10 genes). By CGC Genetics (Portugal). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Hypotrichosis Comprehensive panel. By Connective Tissue Gene Tests (United States). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Hypotrichosis NGS panel. By Connective Tissue Gene Tests (United States). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Hypotrichosis Deletion / Duplication panel. By Connective Tissue Gene Tests (United States). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Nonsyndromic hypotrichosis panel. By Centogene AG - the Rare Disease Company (Germany). RPL21, SNRPE, LPAR6, APCDD1, CDSN, LIPH, DSG4, KRT71, KRT74, HR Specificity 10 % Genes 100 %
Autosomal dominant woolly hair with hypotrichosis. By Centogene AG - the Rare Disease Company (Germany). KRT71 Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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