Generalized hypopigmentation of hair
Symptom Information:
Symptom ID: | HPO:0011358 | ||||
Synonyms: |
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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) Abnormality of hair pigmentation(HPO:0009887) Hypopigmentation of hair(HPO:0005599) Generalized hypopigmentation of hair(HPO:0011358) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Classical phenylketonuria | (Orphanet:79254) |
Menkes disease | (Orphanet:565) |