Hypopigmentation of the skin

Symptom Information:

Symptom ID: HPO:0001010
Synonyms:
Hypopigmentation [HPO:0001010]
Hypopigmented skin [HPO:0001010]
Skin hypopigmentation [HPO:0001010]
Diffuse skin hypopigmentation [Orphanet:23510]
HYPOPIGMENTATION [HPO:0001010]
Hypopigmentation [OMIM:Hypopigmentation]
Hypopigmented skin [OMIM:Hypopigmented skin]
Skin hypopigmentation [OMIM:Skin hypopigmentation]
Diffuse/generalised skin hypopigmentation/cutaneous albinism [Orphanet:23510]
Hypopigmentation (seen only in deletion cases) [OMIM:Hypopigmentation (seen only in deletion cases)]
Albinism [MedDRA:10001557]
Skin albinism [Orphanet:23510]
Albinism (disorder) [Orphanet:23510]
Albinism [Orphanet:23510]
Skin hypopigmentation [MedDRA:10040868]
Quality:
Cross references:
HPO:0007513 "Generalized hypopigmentation" [Orphanet:23510]
Orphanet:23510 "Diffuse/generalised skin hypopigmentation/cutaneous albinism" [Orphanet:23510]
OMIM: "Hypopigmentation" [OMIM:Hypopigmentation]
OMIM: "Hypopigmented skin" [OMIM:Hypopigmented skin]
OMIM: "Skin hypopigmentation" [OMIM:Skin hypopigmentation]
OMIM: "Hypopigmentation (seen only in deletion cases)" [OMIM:Hypopigmentation (seen only in deletion cases)]
UMLS:C1876214 "HYPOPIGMENTATION" [HPO:0001010]
UMLS:C0001916 "Albinism" [Orphanet:23510]
Is a (Direct Parents):
MedDRA Hypopigmentation disorders
HPO         Abnormality of skin pigmentation
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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Pigmentation disorders(MedDRA:10035023)
       Hypopigmentation disorders(MedDRA:10021064)
          Hypopigmentation of the skin(HPO:0001010)
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

Angelman syndrome (Orphanet:72)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Buschke-Ollendorff syndrome (Orphanet:1306)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Chédiak-Higashi syndrome (Orphanet:167)
Classical homocystinuria (Orphanet:394)
Congenital erythropoietic porphyria (Orphanet:79277)
Cystinosis (Orphanet:213)
DILUTION, PIGMENTARY (OMIM:126070)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
FACES syndrome (Orphanet:1969)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Galloway-Mowat syndrome (Orphanet:2065)
Griscelli disease (Orphanet:381)
Griscelli disease type 1 (Orphanet:79476)
Griscelli disease type 2 (Orphanet:79477)
Griscelli disease type 3 (Orphanet:79478)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome type 9 (Orphanet:280663)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Hypertrichosis (Orphanet:79365)
Linear nevus sebaceus syndrome (Orphanet:2612)
Maternal hyperphenylalaninemia (Orphanet:2209)
Menkes disease (Orphanet:565)
Microcephaly-albinism-digital anomalies (Orphanet:2513)
Minimal pigment oculocutaneous albinism type 1 (Orphanet:352734)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebral hypopigmentation syndrome, Preus type (Orphanet:2720)
Oculocerebrorenal syndrome (Orphanet:534)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 1B (Orphanet:79434)
Oculocutaneous albinism type 4 (Orphanet:79435)
Odonto-tricho-ungual-digito-palmar syndrome (Orphanet:69082)
Osteoporosis - oculocutaneous hypopigmentation syndrome (Orphanet:2786)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Prader-Willi syndrome (Orphanet:739)
Primary immunodeficiency syndrome due to p14 deficiency (Orphanet:90023)
RAINDROP HYPOPIGMENTATION (OMIM:179500)
Tietz syndrome (Orphanet:42665)
Vici syndrome (Orphanet:1493)
Xeroderma pigmentosum complementation group C (Orphanet:276255)