Hypotrichosis 13; Hypt13

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 %

You can get up to 4 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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