Hypotrichosis simplex of the scalp
General Information (adopted from Orphanet):
Synonyms, Signs: |
Hereditary hypotrichosis simplex of the scalp |
Number of Symptoms | 2 |
OrphanetNr: | 90368 |
OMIM Id: |
146520
613981 |
ICD-10: |
L65.8 |
UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Autosomal dominant [Orphanet] |
Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Alopecia
-Rare genetic disease -Rare skin disease |
Symptom Information:
|
(HPO:0004782) | Hypotrichosis of the scalp | 7 / 7739 | ||||
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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