Pure hair and nail ectodermal dysplasia

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Pure hair and nail ectodermal dysplasia

ORPHA:69084Malformation syndrome

Also called HNED · Hair-nail ectodermal dysplasia · PHNED

What it is

Pure hair and nail ectodermal dysplasia is characterised by the association of onychodystrophy and severe hypotrichosis, which is mainly limited to the scalp but may also affect the eyelashes and eyebrows. Less than 20 cases have been reported so far. The mode of transmission is autosomal dominant.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Infancy, Neonatal
Inheritance
Autosomal dominant, Autosomal recessive
Classified as
Malformation syndrome

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Genes

HOXC13Disease-causing germline mutation(s) (loss of function)
KRT74Disease-causing germline mutation(s) (loss of function)
KRT85Disease-causing germline mutation(s)

ICD-10 codes

Q82.8filed under a broader ICD-10 category — shared with 106 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MESH C566592MONDO 0019071OMIM 602032OMIM 614927OMIM 614928OMIM 614929OMIM 614931UMLS C4024880

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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