Trichorrhexis nodosa

Symptom Information:

Symptom ID: HPO:0009886
Synonyms:
Brittle hair [Orphanet:24680]
Trichorrhexis (disorder) [Orphanet:24680]
Bamboo hair (disorder) [Orphanet:24680]
Brittle hair (disorder) [Orphanet:24680]
Trichorrhexis [Orphanet:24680]
Trichorrhexis nodosa [OMIM:Trichorrhexis nodosa]
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:0002299 "Brittle hair" [Orphanet:24680]
HPO:0004779 "Brittle scalp hair" [Orphanet:24680]
HPO:0001808 "Fragile nails" [Orphanet:24680]
Orphanet:24680 "Brittle hair/distrix/trichorrhexis" [Orphanet:24680]
OMIM: "Trichorrhexis nodosa" [OMIM:Trichorrhexis nodosa]
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):
MedDRA Pilar disorders NEC
HPO         Abnormal hair laboratory examination
Orphanet Abnormality of hair texture
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)
                   Trichorrhexis nodosa(HPO:0009886)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Pilar disorders NEC(MedDRA:10035035)
          Trichorrhexis nodosa(HPO:0009886)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Argininosuccinic aciduria (Orphanet:23)
Bazex-Dupré-Christol syndrome (Orphanet:113)
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA (OMIM:258360)
Pearson syndrome (Orphanet:699)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Syndromic diarrhea (Orphanet:84064)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 (OMIM:234050)
Trichodysplasia - xeroderma (Orphanet:3361)