Generalized hypopigmentation

Symptom Information:

Symptom ID: HPO:0007513
Synonyms:
Fair skin [HPO:0007513]
Pale pigmentation [HPO:0007513]
Diffuse skin hypopigmentation [Orphanet:23510]
Fair skin [OMIM:Fair skin]
Generalized hypopigmentation [OMIM:Generalized hypopigmentation]
Pale pigmentation [OMIM:Pale pigmentation]
Diffuse/generalised skin hypopigmentation/cutaneous albinism [Orphanet:23510]
Albinism [MedDRA:10001557]
Skin albinism [Orphanet:23510]
Albinism (disorder) [Orphanet:23510]
Albinism [Orphanet:23510]
Quality:
Cross references:
HPO:0001010 "Hypopigmentation of the skin" [Orphanet:23510]
Orphanet:23510 "Diffuse/generalised skin hypopigmentation/cutaneous albinism" [Orphanet:23510]
OMIM: "Fair skin" [OMIM:Fair skin]
OMIM: "Generalized hypopigmentation" [OMIM:Generalized hypopigmentation]
OMIM: "Pale pigmentation" [OMIM:Pale pigmentation]
UMLS:C0001916 "Albinism" [Orphanet:23510]
Is a (Direct Parents):
Orphanet Hypopigmentation of the skin
HPO         Hypopigmentation of the skin
Orphanet Abnormality of skin pigmentation
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:
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)