Premature graying of hair
Symptom Information:
Symptom ID: | HPO:0002216 | ||||||||||||||||
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 pigmentation(HPO:0009887) Premature graying of hair(HPO:0002216) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Prematurely aged appearance(HPO:0007495) Premature graying of hair(HPO:0002216) MedDRA: |
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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) |