Pili torti
Symptom Information:
Symptom ID: | HPO:0003777 | ||||
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) Abnormal hair laboratory examination(HPO:0003328) Pili torti(HPO:0003777) MedDRA: |
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Database Frequency: | 24 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acromelanosis | (Orphanet:39) |
Bamforth syndrome | (Orphanet:1226) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Björnstad syndrome | (Orphanet:123) |
Crandall syndrome | (Orphanet:202) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
GRACILE syndrome | (Orphanet:53693) |
HYPOTRICHOSIS 6 | (OMIM:607903) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
Marie Unna hereditary hypotrichosis | (Orphanet:444) |
Pili torti | (Orphanet:2889) |
Pili torti - developmental delay - neurological abnormalities | (Orphanet:2891) |
Pure hair and nail ectodermal dysplasia | (Orphanet:69084) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Werner syndrome | (Orphanet:902) |
Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |