Brittle hair
Symptom Information:
Symptom ID: | HPO:0002299 | ||||||||||||
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 texture(HPO:0010719) Brittle hair(HPO:0002299) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Pilar disorders NEC(MedDRA:10035035) Brittle hair(HPO:0002299) |
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Database Frequency: | 52 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Argininosuccinic aciduria | (Orphanet:23) |
Björnstad syndrome | (Orphanet:123) |
Brain malformation - congenital heart disease - postaxial polydactyly | (Orphanet:75389) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Classical homocystinuria | (Orphanet:394) |
Crandall syndrome | (Orphanet:202) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE | (OMIM:614929) |
Ectodermal dysplasia - sensorineural deafness | (Orphanet:1883) |
Focal dermal hypoplasia | (Orphanet:2092) |
GRACILE syndrome | (Orphanet:53693) |
Generalized peeling skin syndrome | (Orphanet:263543) |
HYPOTRICHOSIS 6 | (OMIM:607903) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Monilethrix | (Orphanet:573) |
Naxos disease | (Orphanet:34217) |
Netherton syndrome | (Orphanet:634) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Peeling skin syndrome | (Orphanet:817) |
Pili torti | (Orphanet:2889) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Pure hair and nail ectodermal dysplasia | (Orphanet:69084) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Renpenning syndrome | (Orphanet:3242) |
SABINAS BRITTLE HAIR SYNDROME | (OMIM:211390) |
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY | (OMIM:616084) |
Syndromic diarrhea | (Orphanet:84064) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 | (OMIM:234050) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
Trichodental syndrome | (Orphanet:3351) |
Trichodermal syndrome - intellectual deficit | (Orphanet:3360) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Woolly hair | (Orphanet:170) |
Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
X-linked intellectual deficit, Golabi-Ito-Hall type | (Orphanet:93947) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |