Disease Browser
Parent Node: Craniofacial Abnormalities (D019465) Parent Node: Hearing Loss (D034381) Parent Node: Mental Retardation, X-Linked (D038901) ..Starting node .. Abidi X-linked mental retardation syndrome (C535556) Child Nodes:
Sister Nodes: ..Abidi X-linked mental retardation syndrome (C535556) ..Adrenoleukodystrophy (D000326) 4 ..Aldred syndrome (C537046) ..Allan-Herndon-Dudley syndrome (C537047) ..Arena syndrome (C537428) ..Armfield X-Linked Mental Retardation Syndrome (C564551) ..Atkin syndrome (C538195) ..ATR-X syndrome (C538258) ..Borjeson-Forssman-Lehmann syndrome (C536575) ..Brooks-Wisniewski-Brown Syndrome (C563154) ..Chromosome Xp11.3 Deletion Syndrome (C564481) ..CK SYNDROME (OMIM:300831) ..Clark-Baraitser syndrome (C536208) ..Classical Lissencephalies and Subcortical Band Heterotopias (D054221) 5 ..Coffin-Lowry Syndrome (D038921) ..Cowchock syndrome (C536450) ..Creatine deficiency, X-linked (C535598) ..Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations (C566878) ..Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder (C564427) ..Fragile X Syndrome (D005600) 3 ..Glycogen Storage Disease Type IIb (D052120) ..Lesch-Nyhan Syndrome (D007926) 1 ..Lubs X-linked mental retardation syndrome (C537723) ..Lujan Fryns syndrome (C537724) ..MEHMO syndrome (C537451) ..Menkes Kinky Hair Syndrome (D007706) 1 ..Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia (C567466) ..Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism (C564724) ..Mental retardation X-linked syndromic 7 (C537449) ..Mental retardation X-linked, South African type (C537450) ..Mental Retardation, X-Linked 1 (C567906) ..Mental retardation, X-linked 14 (C537454) ..Mental Retardation, X-Linked 16 (C563139) ..Mental Retardation, X-Linked 17 (C563140) ..Mental Retardation, X-Linked 19 (C563141) ..Mental Retardation, X-Linked 2 (C563135) ..Mental Retardation, X-Linked 20 (C563142) ..MENTAL RETARDATION, X-LINKED 21 (OMIM:300143) ..Mental Retardation, X-Linked 23 (C563144) ..Mental Retardation, X-Linked 3 (C563136) ..Mental Retardation, X-Linked 30 (C563146) ..Mental Retardation, X-Linked 31 (C563147) ..Mental Retardation, X-Linked 34 (C563148) ..Mental Retardation, X-Linked 42 (C564524) ..Mental Retardation, X-Linked 45 (C564503) ..Mental Retardation, X-Linked 46 (C564513) ..Mental Retardation, X-Linked 47 (C563151) ..MENTAL RETARDATION, X-LINKED 49 (OMIM:300114) ..Mental Retardation, X-Linked 50 (C564713) ..Mental Retardation, X-Linked 52 (C564502) ..Mental Retardation, X-Linked 53 (C564533) ..Mental Retardation, X-Linked 58 (C564566) ..Mental Retardation, X-Linked 59 (C564470) ..Mental Retardation, X-Linked 63 (C564522) ..Mental Retardation, X-Linked 72 (C564547) ..Mental Retardation, X-Linked 73 (C564528) ..Mental Retardation, X-Linked 77 (C564511) ..Mental Retardation, X-Linked 78 (C564489) ..Mental Retardation, X-Linked 79 (C566876) ..Mental Retardation, X-Linked 81 (C564515) ..Mental Retardation, X-Linked 82 (C564496) ..Mental Retardation, X-Linked 84 (C564501) ..Mental Retardation, X-Linked 89 (C564036) ..Mental Retardation, X-Linked 9 (C563137) ..Mental Retardation, X-Linked 91 (C564482) ..Mental Retardation, X-Linked 92 (C564483) ..Mental Retardation, X-Linked 93 (C567066) ..Mental Retardation, X-Linked 94 (C567479) ..Mental Retardation, X-Linked 95 (C567470) ..MENTAL RETARDATION, X-LINKED 96 (OMIM:300802) ..Mental Retardation, X-Linked Nonsyndromic (C564490) ..Mental Retardation, X-Linked, Syndromic 10 (C564560) ..Mental Retardation, X-Linked, Syndromic 13 (C566875) ..Mental Retardation, X-Linked, Syndromic 14 (C567063) ..Mental retardation, X-linked, syndromic 5 (C535773) ..Mental Retardation, X-Linked, Syndromic 9 (C567474) ..Mental Retardation, X-Linked, Syndromic, Jarid1c-Related (C564494) ..MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE (OMIM:300799) ..Mental Retardation, X-Linked, Syndromic, Ube2a-Related (C564069) ..Mental Retardation, X-Linked, Syp-Related (C567584) ..Mental Retardation, X-Linked, With Brachydactyly And Macroglossia (C567069) ..Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance (C537456) ..Mental Retardation, X-Linked, with Epilepsy (C564516) ..Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency (C564712) ..Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related (C563150) ..Mental Retardation, X-Linked, with Short Stature (C564527) ..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354) ..Mental Retardation, X-Linked, With Spasticity (C566877) ..Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457) ..Microphthalmia, Syndromic 4 (C564457) ..Miles-Carpenter x-linked mental retardation syndrome (C537472) ..Mucopolysaccharidosis II (D016532) ..Opitz-Kaveggia syndrome (C537923) ..Orofaciodigital syndrome, Shashi type (C537135) ..Partington X-linked mental retardation syndrome (C536300) ..Plagiocephaly and X-linked mental retardation (C537512) ..Ppm-X Syndrome (C580387) ..Prieto X-linked mental retardation syndrome (C535274) ..Pyruvate Dehydrogenase Complex Deficiency Disease (D015325) 4 ..Renpenning syndrome 1 (C537761) ..Rett Syndrome (D015518) 5 ..Roifman syndrome (C535866) ..Schimke X-linked mental retardation syndrome (C536630) ..Siderius X-linked mental retardation syndrome (C537333) ..Snyder Robinson syndrome (C536678) ..Stocco dos Santos syndrome (C537495) ..Tranebjaerg Svejgaard syndrome (C536978) ..Wilson-Turner X-linked mental retardation syndrome (C536708) ..Wittwer syndrome (C536737) ..X-linked mental retardation Gustavson type (C536759) ..X-linked mental retardation type Wittwer (C536760) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 80
Name: Abidi X-linked mental retardation syndrome
Definition:
Alternative IDs: OMIM:300262
ParentIDs: MESH:D019465|MESH:D034381|MESH:D038901
TreeNumbers: C05.660.207/C535556 |C09.218.458.341/C535556 |C10.597.606.643.455/C535556 |C10.597.751.418.341/C535556 |C16.131.621.207/C535556 |C16.320.322.500/C535556 |C16.320.400.525/C535556 |C23.888.592.763.393.341/C535556
Synonyms: Mental retardation X-linked, Abidi type |Mental Retardation, X-Linked, Abidi Type |MENTAL RETARDATION, X-LINKED, SYNDROMIC, ABIDI TYPE |MRXSAB |Short stature, small head circumference, sloping forehead, hearing loss, cupped ears and small testes
Slim Mappings: Congenital abnormality|Ear-nose-throat disease|Genetic disease (inborn)|Musculoskeletal disease|Nervous system disease|Signs and symptoms
Reference:
MedGen: C535556
MeSH: C535556
OMIM: 300262 ; Genes: Phenotypes Disease Causing ClinVar Variants