| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Craniofacial Abnormalities (D019465) |
Parent Node:
Pigmentation Disorders (D010859) |
..Starting node
.. Oculocerebral hypopigmentation syndrome type Preus (C537866)
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Child Nodes:
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Sister Nodes: |
..Acroleukopathy, Symmetric (C566322)
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..Anonychia with Flexural Pigmentation (C566278)
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..Argyria (D001129)
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..BADS Syndrome (C562663)
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..Basaran Yilmaz syndrome (C537660)
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..Bullous Dystrophy, Hereditary Macular Type (C563065)
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..Cafe-au-Lait Spots (D019080)  4
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..Dyschromatosis symmetrica hereditaria 1 (C535729)
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..Dyschromatosis universalis hereditaria (C535730)
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..Dyschromatosis Universalis Hereditaria 1 (C567273)
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..Dyschromatosis Universalis Hereditaria 2 (C567194)
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..Elejalde Disease (C536203)
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..FLOTCH syndrome (C537065)
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..Graying of Hair, Precocious (C564209)
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..Griscelli syndrome type 1 (C537301)
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..Griscelli syndrome type 3 (C537303)
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..Grouped Pigmentation of the Macula (C565530)
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..Heterochromia iridis (C538115)
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..Hyperpigmentation (D017495) 30
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..Hypopigmentation (D017496) 49
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..Incontinentia Pigmenti (D007184) 2
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..Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
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..Macules hereditary congenital hypopigmented and hyperpigmented (C537836)
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..Oculocerebral hypopigmentation syndrome type Preus (C537866)
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..Peeling skin syndrome, acral type (C536316)
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..Pigmentary Disorder, Reticulate, with Systemic Manifestations (C564461)
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..Pigmented purpuric eruption (C537186)
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..Propping Zerres syndrome (C538052)
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..Red skin pigment anomaly of New Guinea (C535515)
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..Russell-Silver Syndrome, X-Linked (C562446)
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..Skin/Hair/Eye Pigmentation, Variation In, 10 (C567376)
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..Skin/Hair/Eye Pigmentation, Variation In, 11 (C567374)
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..Skin/Hair/Eye Pigmentation, Variation In, 4 (C567300)
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..Skin/Hair/Eye Pigmentation, Variation In, 5 (C567119)
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..Skin/Hair/Eye Pigmentation, Variation In, 6 (C567139)
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..Skin/Hair/Eye Pigmentation, Variation In, 7 (C567155)
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..Skin/Hair/Eye Pigmentation, Variation In, 8 (C567096)
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..Skin/Hair/Eye Pigmentation, Variation In, 9 (C567091)
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..Spastic paraplegia 23 (C536859)
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..Tang Hsi Ryu syndrome (C536897)
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..TERMINAL OSSEOUS DYSPLASIA (OMIM:300244)
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..Terminal Osseous Dysplasia and Pigmentary Defects (C564554)
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..Thumb deformity, alopecia, pigmentation anomaly (C536904)
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..Urticaria Pigmentosa (D014582)
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..WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580)
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..White forelock with malformations (C536700)
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..Whyte Murphy syndrome (C536054)
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..Xeroderma Pigmentosum (D014983) 16
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..Yellow Nail Syndrome (D056684) 1
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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