Absent skin pigmentation
Symptom Information:
Symptom ID: | HPO:0200098 | ||||
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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) Hypopigmentation of the skin(HPO:0001010) Absent skin pigmentation(HPO:0200098) MedDRA: |
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Database Frequency: | 2 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Oculocutaneous albinism type 1 | (Orphanet:352731) |
Oculocutaneous albinism type 1A | (Orphanet:79431) |