Slow-growing hair
Symptom Information:
Symptom ID: | HPO:0002217 | |||||
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 growth rate(HPO:0011363) Slow-growing hair(HPO:0002217) MedDRA: |
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Database Frequency: | 22 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Monilethrix | (Orphanet:573) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Oculodentodigital dysplasia | (Orphanet:2710) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Trichodental syndrome | (Orphanet:3351) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
WOOLLY HAIR, AUTOSOMAL DOMINANT | (OMIM:194300) |
Woolly hair | (Orphanet:170) |