Hypopigmentation of hair
Symptom Information:
Symptom ID: | HPO:0005599 | ||||
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 skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of hair pigmentation(HPO:0009887) Hypopigmentation of hair(HPO:0005599) MedDRA: |
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Database Frequency: | 38 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Classical phenylketonuria | (Orphanet:79254) |
Cystinosis | (Orphanet:213) |
DILUTION, PIGMENTARY | (OMIM:126070) |
Deaf blind hypopigmentation syndrome, Yemenite type | (Orphanet:3214) |
Griscelli disease type 2 | (Orphanet:79477) |
Griscelli disease type 3 | (Orphanet:79478) |
Heart defect - round face - congenital developmental delay | (Orphanet:1355) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Menkes disease | (Orphanet:565) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Neuroectodermal melanolysosomal disease | (Orphanet:33445) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculocutaneous albinism | (Orphanet:55) |
Oculocutaneous albinism type 1A | (Orphanet:79431) |
Oculocutaneous albinism type 2 | (Orphanet:79432) |
Oculocutaneous albinism type 4 | (Orphanet:79435) |
Piebald trait - neurologic defects | (Orphanet:2885) |
Piebaldism | (Orphanet:2884) |
Prader-Willi syndrome | (Orphanet:739) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Temperature-sensitive oculocutaneous albinism type 1 | (Orphanet:352737) |
Tietz syndrome | (Orphanet:42665) |
Trichodermal syndrome - intellectual deficit | (Orphanet:3360) |
Vici syndrome | (Orphanet:1493) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Waardenburg syndrome type 2 | (Orphanet:895) |
Waardenburg-Shah syndrome | (Orphanet:897) |
Woolly hair | (Orphanet:170) |
Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |