Facial hypertrichosis

Symptom Information:

Symptom ID: HPO:0002219
Synonyms:
Facial hypertrichosis [OMIM:Facial hypertrichosis]
Quality:
Cross references:
OMIM: "Facial hypertrichosis" [OMIM:Facial hypertrichosis]
Is a (Direct Parents):
HPO         Hypertrichosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormal hair quantity(HPO:0011362)
                   Hypertrichosis(HPO:0000998)
                      Facial hypertrichosis(HPO:0002219)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

COFFIN-SIRIS SYNDROME (OMIM:135900)
Coffin-Siris syndrome (Orphanet:1465)
FACIAL HYPERTRICHOSIS (OMIM:134000)
Hepatoerythropoietic porphyria (Orphanet:95159)
Micro syndrome (Orphanet:2510)
Peters-plus syndrome (Orphanet:709)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
WARBURG MICRO SYNDROME 1 (OMIM:600118)