Brittle hair

Symptom Information:

Symptom ID: HPO:0002299
Synonyms:
Trichorrhexis (disorder) [Orphanet:24680]
Bamboo hair (disorder) [Orphanet:24680]
Brittle hair (disorder) [Orphanet:24680]
Trichorrhexis [Orphanet:24680]
Brittle hair [Orphanet:24680]
Brittle hair [OMIM:Brittle hair]
Brittle hair/distrix/trichorrhexis [Orphanet:24680]
Trichorrhexis [MedDRA:10044625]
Split ends [MedDRA:10044625]
Trichorrhexis nodosa [MedDRA:10044625]
Hair breakage [MedDRA:10044625]
Brittle hair (in some patients) [OMIM:Brittle hair (in some patients)]
Quality:
Cross references:
HPO:0004779 "Brittle scalp hair" [Orphanet:24680]
HPO:0009886 "Trichorrhexis nodosa" [Orphanet:24680]
HPO:0001808 "Fragile nails" [Orphanet:24680]
Orphanet:24680 "Brittle hair/distrix/trichorrhexis" [Orphanet:24680]
OMIM: "Brittle hair" [OMIM:Brittle hair]
OMIM: "Brittle hair (in some patients)" [OMIM:Brittle hair (in some patients)]
UMLS:C0702163 "Trichorrhexis" [Orphanet:24680]
UMLS:C0263490 "Brittle hair" [Orphanet:24680]
Is a (Direct Parents):
Orphanet Abnormality of hair texture
HPO         Abnormality of hair texture
MedDRA Pilar disorders NEC
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)
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)