Acquired hypertrichosis lanuginosa

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 18
OrphanetNr: 2221
OMIM Id:
ICD-10: L68.1
UMLs:
MeSH:
MedDRA:
Snomed: 25967007

Prevalence, inheritance and age of onset:

Prevalence: 60 cases [Orphanet]
Inheritance: Not applicable
[Orphanet]
Age of onset: Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Hypertrichosis
 -Rare genetic disease
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0100615) Ovarian neoplasm Occasional [Orphanet] 25 / 7739
2
 (HPO:0000206) Glossitis Frequent [Orphanet] 9 / 7739
3
 (HPO:0000606) Abnormality of the periorbital region Very frequent [Orphanet] 96 / 7739
4
 (HPO:0000158) Macroglossia Frequent [Orphanet] 119 / 7739
5
 (HPO:0000534) Abnormality of the eyebrow Very frequent [Orphanet] 39 / 7739
6
 (HPO:0100013) Neoplasm of the breast Occasional [Orphanet] 18 / 7739
7
 (HPO:0002024) Malabsorption Occasional [Orphanet] 142 / 7739
8
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
9
 (HPO:0000956) Acanthosis nigricans Occasional [Orphanet] 54 / 7739
10
 (HPO:0008064) Ichthyosis Occasional [Orphanet] 108 / 7739
11
 (HPO:0002213) Fine hair Very frequent [Orphanet] 77 / 7739
12
 (HPO:0005599) Hypopigmentation of hair Very frequent [Orphanet] 38 / 7739
13
 (HPO:0011362) Abnormal hair quantity Very frequent [Orphanet] 92 / 7739
14
 (HPO:0001072) Thickened skin Occasional [Orphanet] 87 / 7739
15
 (HPO:0004540) Congenital, generalized hypertrichosis Very frequent [Orphanet] 11 / 7739
16
 (HPO:0100526) Neoplasm of the lung Occasional [Orphanet] 26 / 7739
17
 (HPO:0002664) Neoplasm Very frequent [Orphanet] 111 / 7739
18
 (HPO:0002716) Lymphadenopathy Occasional [Orphanet] 129 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: