Hypopigmentation of hair

Symptom Information:

Symptom ID: HPO:0005599
Synonyms:
Hair hypopigmentation [HPO:0005599]
Hair hypopigmentation [Orphanet:24280]
Hair hypopigmentation [OMIM:Hair hypopigmentation]
Decreased hair pigmentation/hypopigmentation of hair [Orphanet:24280]
Quality:
Cross references:
HPO:0011358 "Generalized hypopigmentation of hair" [Orphanet:24280]
Orphanet:24280 "Decreased hair pigmentation/hypopigmentation of hair" [Orphanet:24280]
OMIM: "Hair hypopigmentation" [OMIM:Hair hypopigmentation]
Is a (Direct Parents):
Orphanet Abnormality of the hair
HPO         Abnormality of hair pigmentation
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)
                   Hypopigmentation of hair(HPO:0005599)
MedDRA:
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

Acquired hypertrichosis lanuginosa (Orphanet:2221)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Chédiak-Higashi syndrome (Orphanet:167)
Classical phenylketonuria (Orphanet:79254)
Cystinosis (Orphanet:213)
DILUTION, PIGMENTARY (OMIM:126070)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Griscelli disease type 2 (Orphanet:79477)
Griscelli disease type 3 (Orphanet:79478)
Heart defect - round face - congenital developmental delay (Orphanet:1355)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Koolen-De Vries syndrome (Orphanet:96169)
Menkes disease (Orphanet:565)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 4 (Orphanet:79435)
Piebald trait - neurologic defects (Orphanet:2885)
Piebaldism (Orphanet:2884)
Prader-Willi syndrome (Orphanet:739)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Temperature-sensitive oculocutaneous albinism type 1 (Orphanet:352737)
Tietz syndrome (Orphanet:42665)
Trichodermal syndrome - intellectual deficit (Orphanet:3360)
Vici syndrome (Orphanet:1493)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg-Shah syndrome (Orphanet:897)
Woolly hair (Orphanet:170)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)