Fair hair
Symptom Information:
Symptom ID: | HPO:0002286 | |||||
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) Generalized hypopigmentation of hair(HPO:0011358) Fair hair(HPO:0002286) MedDRA: |
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Database Frequency: | 20 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
ADULT syndrome | (Orphanet:978) |
Angelman syndrome | (Orphanet:72) |
Cartilage-hair hypoplasia | (Orphanet:175) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
Hypotrichosis simplex | (Orphanet:55654) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Loose anagen syndrome | (Orphanet:168) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Monosomy 9p | (Orphanet:261112) |
Oculocutaneous albinism type 7 | (Orphanet:352745) |
Phenylketonuria | (Orphanet:716) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |
Urocanic aciduria | (Orphanet:210128) |