Hypopigmentation of the skin
Symptom Information:
Symptom ID: | HPO:0001010 | |||||||||||||||
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 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) |
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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) |