Abnormal hair whorl
Symptom Information:
Symptom ID: | HPO:0010721 | ||
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 pattern(HPO:0010720) Congenital abnormal hair pattern(HPO:0011361) Abnormal hair whorl(HPO:0010721) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Werner syndrome | (Orphanet:902) |