Generalized hypopigmentation
Symptom Information:
Symptom ID: | HPO:0007513 | |||||||||||
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) Generalized hypopigmentation(HPO:0007513) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Menkes disease | (Orphanet:565) |
OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS | (OMIM:257790) |
Phenylketonuria | (Orphanet:716) |
Prader-Willi syndrome | (Orphanet:739) |
Tietz syndrome | (Orphanet:42665) |