Facial hypertrichosis
Symptom Information:
Symptom ID: | HPO:0002219 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |