| Disease Browser
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Parent Node:
 Ectodermal Dysplasia (D004476) |
Parent Node:
Nails, Malformed (D009264) |
..Starting node
.. Basan syndrome (C537659)
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Child Nodes:
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Sister Nodes: |
..Alopecia universalis onychodystrophy vitiligo (C537056)
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..Ameloonychohypohidrotic syndrome (C538245)
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..Anonychia congenita (C536377)
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..Anonychia onychodystrophy (C536378)
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..Anonychia with Flexural Pigmentation (C566278)
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..Anonychia, Total, with Microcephaly (C564606)
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..Anonychia-Ectrodactyly (C566277)
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..Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly (C536379)
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..Basan syndrome (C537659)
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..Brachymorphism-onychodysplasia-dysphalangism syndrome (C536242)
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..Cartwright Nelson Fryns syndrome (C535917)
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..Curly hair-acral keratoderma-caries syndrome (C536220)
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..Curly hair-ankyloblepharon-nail dysplasia syndrome (C538074)
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..Deafness enamel hypoplasia nail defects (C535994)
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..Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274)
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..Dermoodontodysplasia (C565103)
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..Digitorenocerebral Syndrome (C563052)
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..Double Nail for Fifth Toe (C565090)
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..Gorlin Bushkell Jensen syndrome (C537289)
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..Hereditary koilonychia (C537260)
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..Hypospadias-Mental Retardation Syndrome (C563067)
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..MAMMARY-DIGITAL-NAIL SYNDROME (OMIM:613689)
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..NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 (OMIM:614149)
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..Oculotrichodysplasia (C564934)
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..Onycholysis, Partial, with Scleronychia (C563503)
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..Onychotrichodysplasia and neutropenia (C537752)
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..Otoonychoperoneal Syndrome (C564912)
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..Pili torti onychodysplasia (C537399)
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..Pinheiro Freire-Maia Miranda syndrome (C537402)
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..Propping Zerres syndrome (C538052)
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..Santos Syndrome (C567819)
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..Schinzel-Giedion syndrome (C536632)
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..Steatocystoma multiplex with natal teeth (C537487)
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..Teebi Kaurah syndrome (C536948)
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..Temple-Baraitser Syndrome (C567516)
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..Toenail Dystrophy, Isolated (C564384)
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..Tonoki syndrome (C536967)
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..Twenty-Nail Dystrophy (C562907)
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..Ulna hypoplasia with mental retardation (C536934)
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..Ulnar Hypoplasia with Mental Retardation (C564757)
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..Witkop syndrome (C536736)
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..Yellow Nail Syndrome (D056684)  1
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..Zori Stalker Williams syndrome (C536728)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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