Aplasia cutis congenita of midline scalp vertex
Symptom Information:
Symptom ID: | HPO:0007536 | ||
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 the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Aplasia/Hypoplasia of the skin(HPO:0008065) Aplasia cutis congenita(HPO:0001057) Aplasia cutis congenita of scalp(HPO:0007385) Aplasia cutis congenita over the scalp vertex(HPO:0004471) Aplasia cutis congenita of midline scalp vertex(HPO:0007536) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Aplasia cutis - myopia | (Orphanet:1117) |