| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Attention Deficit Disorder with Hyperactivity (D001289) |
Parent Node:
Mental Retardation, X-Linked (D038901) |
..Starting node
.. Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder (C564427)
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Child Nodes:
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Sister Nodes: |
..Abidi X-linked mental retardation syndrome (C535556)
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..Adrenoleukodystrophy (D000326)  4
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..Aldred syndrome (C537046)
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..Allan-Herndon-Dudley syndrome (C537047)
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..Arena syndrome (C537428)
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..Armfield X-Linked Mental Retardation Syndrome (C564551)
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..Atkin syndrome (C538195)
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..ATR-X syndrome (C538258)
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..Borjeson-Forssman-Lehmann syndrome (C536575)
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..Brooks-Wisniewski-Brown Syndrome (C563154)
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..Chromosome Xp11.3 Deletion Syndrome (C564481)
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..CK SYNDROME (OMIM:300831)
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..Clark-Baraitser syndrome (C536208)
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..Classical Lissencephalies and Subcortical Band Heterotopias (D054221) 5
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..Coffin-Lowry Syndrome (D038921)
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..Cowchock syndrome (C536450)
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..Creatine deficiency, X-linked (C535598)
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..Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations (C566878)
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..Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder (C564427)
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..Fragile X Syndrome (D005600) 3
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..Glycogen Storage Disease Type IIb (D052120)
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..Lesch-Nyhan Syndrome (D007926) 1
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..Lubs X-linked mental retardation syndrome (C537723)
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..Lujan Fryns syndrome (C537724)
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..MEHMO syndrome (C537451)
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..Menkes Kinky Hair Syndrome (D007706) 1
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..Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia (C567466)
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..Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism (C564724)
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..Mental retardation X-linked syndromic 7 (C537449)
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..Mental retardation X-linked, South African type (C537450)
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..Mental Retardation, X-Linked 1 (C567906)
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..Mental retardation, X-linked 14 (C537454)
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..Mental Retardation, X-Linked 16 (C563139)
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..Mental Retardation, X-Linked 17 (C563140)
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..Mental Retardation, X-Linked 19 (C563141)
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..Mental Retardation, X-Linked 2 (C563135)
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..Mental Retardation, X-Linked 20 (C563142)
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..MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
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..Mental Retardation, X-Linked 23 (C563144)
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..Mental Retardation, X-Linked 3 (C563136)
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..Mental Retardation, X-Linked 30 (C563146)
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..Mental Retardation, X-Linked 31 (C563147)
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..Mental Retardation, X-Linked 34 (C563148)
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..Mental Retardation, X-Linked 42 (C564524)
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..Mental Retardation, X-Linked 45 (C564503)
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..Mental Retardation, X-Linked 46 (C564513)
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..Mental Retardation, X-Linked 47 (C563151)
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..MENTAL RETARDATION, X-LINKED 49 (OMIM:300114)
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..Mental Retardation, X-Linked 50 (C564713)
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..Mental Retardation, X-Linked 52 (C564502)
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..Mental Retardation, X-Linked 53 (C564533)
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..Mental Retardation, X-Linked 58 (C564566)
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..Mental Retardation, X-Linked 59 (C564470)
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..Mental Retardation, X-Linked 63 (C564522)
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..Mental Retardation, X-Linked 72 (C564547)
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..Mental Retardation, X-Linked 73 (C564528)
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..Mental Retardation, X-Linked 77 (C564511)
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..Mental Retardation, X-Linked 78 (C564489)
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..Mental Retardation, X-Linked 79 (C566876)
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..Mental Retardation, X-Linked 81 (C564515)
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..Mental Retardation, X-Linked 82 (C564496)
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..Mental Retardation, X-Linked 84 (C564501)
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..Mental Retardation, X-Linked 89 (C564036)
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..Mental Retardation, X-Linked 9 (C563137)
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..Mental Retardation, X-Linked 91 (C564482)
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..Mental Retardation, X-Linked 92 (C564483)
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..Mental Retardation, X-Linked 93 (C567066)
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..Mental Retardation, X-Linked 94 (C567479)
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..Mental Retardation, X-Linked 95 (C567470)
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..MENTAL RETARDATION, X-LINKED 96 (OMIM:300802)
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..Mental Retardation, X-Linked Nonsyndromic (C564490)
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..Mental Retardation, X-Linked, Syndromic 10 (C564560)
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..Mental Retardation, X-Linked, Syndromic 13 (C566875)
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..Mental Retardation, X-Linked, Syndromic 14 (C567063)
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..Mental retardation, X-linked, syndromic 5 (C535773)
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..Mental Retardation, X-Linked, Syndromic 9 (C567474)
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..Mental Retardation, X-Linked, Syndromic, Jarid1c-Related (C564494)
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..MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE (OMIM:300799)
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..Mental Retardation, X-Linked, Syndromic, Ube2a-Related (C564069)
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..Mental Retardation, X-Linked, Syp-Related (C567584)
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..Mental Retardation, X-Linked, With Brachydactyly And Macroglossia (C567069)
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..Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance (C537456)
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..Mental Retardation, X-Linked, with Epilepsy (C564516)
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..Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency (C564712)
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..Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related (C563150)
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..Mental Retardation, X-Linked, with Short Stature (C564527)
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..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
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..Mental Retardation, X-Linked, With Spasticity (C566877)
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..Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457)
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..Microphthalmia, Syndromic 4 (C564457)
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..Miles-Carpenter x-linked mental retardation syndrome (C537472)
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..Mucopolysaccharidosis II (D016532)
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..Opitz-Kaveggia syndrome (C537923)
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..Orofaciodigital syndrome, Shashi type (C537135)
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..Partington X-linked mental retardation syndrome (C536300)
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..Plagiocephaly and X-linked mental retardation (C537512)
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..Ppm-X Syndrome (C580387)
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..Prieto X-linked mental retardation syndrome (C535274)
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..Pyruvate Dehydrogenase Complex Deficiency Disease (D015325) 4
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..Renpenning syndrome 1 (C537761)
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..Rett Syndrome (D015518) 5
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..Roifman syndrome (C535866)
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..Schimke X-linked mental retardation syndrome (C536630)
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..Siderius X-linked mental retardation syndrome (C537333)
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..Snyder Robinson syndrome (C536678)
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..Stocco dos Santos syndrome (C537495)
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..Tranebjaerg Svejgaard syndrome (C536978)
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..Wilson-Turner X-linked mental retardation syndrome (C536708)
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..Wittwer syndrome (C536737)
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..X-linked mental retardation Gustavson type (C536759)
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..X-linked mental retardation type Wittwer (C536760)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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