Disease Browser
Parent Node: Pigmentation Disorders (D010859) ..Starting node .. Hypopigmentation (D017496) Child Nodes:
........Albinism (D000417) 30 ........External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation (C566509) ........Hernandez Fragoso syndrome (C536062) ........HYPOMELANOSIS OF ITO (OMIM:300337) ........Leukonychia totalis (C535889) ........Raindrop Hypopigmentation (C566724) ........Vitiligo (D014820) 11 ........Yemenite deaf-blind hypopigmentation syndrome (C536771) Sister Nodes: ..Acroleukopathy, Symmetric (C566322) ..Anonychia with Flexural Pigmentation (C566278) ..Argyria (D001129) ..BADS Syndrome (C562663) ..Basaran Yilmaz syndrome (C537660) ..Bullous Dystrophy, Hereditary Macular Type (C563065) ..Cafe-au-Lait Spots (D019080) 4 ..Dyschromatosis symmetrica hereditaria 1 (C535729) ..Dyschromatosis universalis hereditaria (C535730) ..Dyschromatosis Universalis Hereditaria 1 (C567273) ..Dyschromatosis Universalis Hereditaria 2 (C567194) ..Elejalde Disease (C536203) ..FLOTCH syndrome (C537065) ..Graying of Hair, Precocious (C564209) ..Griscelli syndrome type 1 (C537301) ..Griscelli syndrome type 3 (C537303) ..Grouped Pigmentation of the Macula (C565530) ..Heterochromia iridis (C538115) ..Hyperpigmentation (D017495) 30 ..Hypopigmentation (D017496) 49 ..Incontinentia Pigmenti (D007184) 2 ..Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440) ..Macules hereditary congenital hypopigmented and hyperpigmented (C537836) ..Oculocerebral hypopigmentation syndrome type Preus (C537866) ..Peeling skin syndrome, acral type (C536316) ..Pigmentary Disorder, Reticulate, with Systemic Manifestations (C564461) ..Pigmented purpuric eruption (C537186) ..Propping Zerres syndrome (C538052) ..Red skin pigment anomaly of New Guinea (C535515) ..Russell-Silver Syndrome, X-Linked (C562446) ..Skin/Hair/Eye Pigmentation, Variation In, 10 (C567376) ..Skin/Hair/Eye Pigmentation, Variation In, 11 (C567374) ..Skin/Hair/Eye Pigmentation, Variation In, 4 (C567300) ..Skin/Hair/Eye Pigmentation, Variation In, 5 (C567119) ..Skin/Hair/Eye Pigmentation, Variation In, 6 (C567139) ..Skin/Hair/Eye Pigmentation, Variation In, 7 (C567155) ..Skin/Hair/Eye Pigmentation, Variation In, 8 (C567096) ..Skin/Hair/Eye Pigmentation, Variation In, 9 (C567091) ..Spastic paraplegia 23 (C536859) ..Tang Hsi Ryu syndrome (C536897) ..TERMINAL OSSEOUS DYSPLASIA (OMIM:300244) ..Terminal Osseous Dysplasia and Pigmentary Defects (C564554) ..Thumb deformity, alopecia, pigmentation anomaly (C536904) ..Urticaria Pigmentosa (D014582) ..WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580) ..White forelock with malformations (C536700) ..Whyte Murphy syndrome (C536054) ..Xeroderma Pigmentosum (D014983) 16 ..Yellow Nail Syndrome (D056684) 1 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD