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Alopecia universalis
3 OMIM references -
1 associated gene
8 connected diseases
6 signs/symptoms
Disease Type of connection
Atrichia with papular lesions
Marie Unna hereditary hypotrichosis
Hypocalcemic vitamin D-resistant rickets
Autosomal recessive dopa-responsive dystonia
Peripheral resistance to thyroid hormones
Acute promyelocytic leukemia
Matthew-Wood syndrome
Papillary or follicular thyroid carcinoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Epidemiological data:
(no data available)
External references:
3 OMIM references -
1 MeSH reference: C537055
Gene symbol UniProt reference OMIM reference
HR O43593602302
Very frequent
- Absent / decreased lashes
- Absent / decreased / thin eyebrows
- Alopecia
- Autosomal recessive inheritance
- Decreased body hair / axillar / pubic hairlessness
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness