Premature graying of hair

Symptom Information:

Symptom ID: HPO:0002216
Synonyms:
Early graying [HPO:0002216]
Premature graying [HPO:0002216]
PREMATURE GRAYING OF THE HAIR [HPO:0002216]
Premature greying [HPO:0002216]
Premature hair graying [HPO:0002216]
Premature hair greying [Orphanet:24240]
Premature canities (disorder) [Orphanet:24240]
Premature canities [Orphanet:24240]
Early graying [OMIM:Early graying]
Premature graying [OMIM:Premature graying]
Premature graying of hair [OMIM:Premature graying of hair]
Premature graying of the hair [OMIM:Premature graying of the hair]
Premature greying [OMIM:Premature greying]
Premature hair graying [OMIM:Premature hair graying]
Premature greying of hair [Orphanet:24240]
Premature graying (1 family) [OMIM:Premature graying (1 family)]
Quality:
Cross references:
Orphanet:24240 "Premature greying of hair" [Orphanet:24240]
OMIM: "Early graying" [OMIM:Early graying]
OMIM: "Premature graying" [OMIM:Premature graying]
OMIM: "Premature graying of hair" [OMIM:Premature graying of hair]
OMIM: "Premature graying of the hair" [OMIM:Premature graying of the hair]
OMIM: "Premature greying" [OMIM:Premature greying]
OMIM: "Premature hair graying" [OMIM:Premature hair graying]
OMIM: "Premature graying (1 family)" [OMIM:Premature graying (1 family)]
UMLS:C0263498 "Premature canities" [Orphanet:24240]
Is a (Direct Parents):
HPO         Prematurely aged appearance
HPO         Abnormality of hair pigmentation
Orphanet Abnormality of the hair
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Prematurely aged appearance(HPO:0007495)
                   Premature graying of hair(HPO:0002216)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormality of hair pigmentation(HPO:0009887)
                   Premature graying of hair(HPO:0002216)
MedDRA:
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

Ataxia-telangiectasia (Orphanet:100)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Branchio-oculo-facial syndrome (Orphanet:1297)
Böök syndrome (Orphanet:1262)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Dyskeratosis congenita (Orphanet:1775)
GRAYING OF HAIR, PRECOCIOUS (OMIM:139100)
Griscelli disease (Orphanet:381)
Griscelli disease type 1 (Orphanet:79476)
Griscelli disease type 2 (Orphanet:79477)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Monosomy 5p (Orphanet:281)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 (OMIM:614742)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2 (OMIM:614743)
Rabson-Mendenhall syndrome (Orphanet:769)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Rothmund-Thomson syndrome (Orphanet:2909)
Sensorineural hearing loss - early graying - essential tremor (Orphanet:66633)
TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS (OMIM:190200)
Vogt-Koyanagi-Harada disease (Orphanet:3437)
WAARDENBURG SYNDROME, TYPE 2A (OMIM:193510)
WAARDENBURG SYNDROME, TYPE 2B (OMIM:600193)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580)
WAARDENBURG SYNDROME, TYPE 4B (OMIM:613265)
WAARDENBURG SYNDROME, TYPE 4C (OMIM:613266)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg syndrome type 3 (Orphanet:896)
Waardenburg-Shah syndrome (Orphanet:897)
Williams syndrome (Orphanet:904)