White forelock
Symptom Information:
Symptom ID: | HPO:0002211 | |||||
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) Patchy hypopigmentation of hair(HPO:0011365) White forelock(HPO:0002211) MedDRA: |
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Database Frequency: | 18 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Deaf blind hypopigmentation syndrome, Yemenite type | (Orphanet:3214) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Piebald trait - neurologic defects | (Orphanet:2885) |
Piebaldism | (Orphanet:2884) |
WAARDENBURG SYNDROME, TYPE 2A | (OMIM:193510) |
WAARDENBURG SYNDROME, TYPE 2B | (OMIM:600193) |
WAARDENBURG SYNDROME, TYPE 2E | (OMIM:611584) |
WAARDENBURG SYNDROME, TYPE 4A | (OMIM:277580) |
WAARDENBURG SYNDROME, TYPE 4B | (OMIM:613265) |
WAARDENBURG SYNDROME, TYPE 4C | (OMIM:613266) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Waardenburg syndrome type 2 | (Orphanet:895) |
Waardenburg syndrome type 3 | (Orphanet:896) |
Waardenburg-Shah syndrome | (Orphanet:897) |
Werner syndrome | (Orphanet:902) |
White forelock with malformations | (Orphanet:2475) |