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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Mental Retardation, X-Linked (D038901)
..Starting node ..Snyder Robinson syndrome (C536678)
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:

10335

Name:

Snyder Robinson syndrome

Definition:

Alternative IDs:

OMIM:309583

ParentIDs:

MESH:D038901

TreeNumbers:

C10.597.606.643.455/C536678 |C16.320.322.500/C536678 |C16.320.400.525/C536678

Synonyms:

Slim Mappings:

Genetic disease (inborn)|Nervous system disease

Reference:

MedGen: C536678
MeSH: C536678
OMIM: 309583;

Genes: SMS;

Phenotypes

1	HP:0001419	X-linked recessive inheritance
2	HP:0000377	Abnormality of the pinna
3	HP:0000193	Bifid uvula
4	HP:0002136	Broad-based gait
5	HP:0000175	Cleft palate
6	HP:0000028	Cryptorchidism
7	HP:0003199	Decreased muscle mass
8	HP:0000678	Dental crowding
9	HP:0001260	Dysarthria
10	HP:0000324	Facial asymmetry
11	HP:0001290	Generalized hypotonia
12	HP:0011003	High myopia
13	HP:0002705	High, narrow palate
14	HP:0001187	Hyperextensibility of the finger joints
15	HP:0000316	Hypertelorism
16	HP:0001252	Hypotonia
17	HP:0001249	Intellectual disability
18	HP:0002751	Kyphoscoliosis
19	HP:0100807	Long fingers
20	HP:0001847	Long hallux
21	HP:0011302	Long palm
22	HP:0000303	Mandibular prognathia
23	HP:0004283	Narrow palm
24	HP:0001611	Nasal speech
25	HP:0000939	Osteoporosis
26	HP:0000768	Pectus carinatum
27	HP:0000767	Pectus excavatum
28	HP:0003812	Phenotypic variability
29	HP:0002757	Recurrent fractures
30	HP:0001250	Seizure
31	HP:0000322	Short philtrum
32	HP:0004322	Short stature
33	HP:0001762	Talipes equinovarus
34	HP:0000098	Tall stature
35	HP:0000179	Thick lower lip vermilion
36	HP:0000465	Webbed neck
37	HP:0006610	Wide intermamillary distance

Disease Causing ClinVar Variants

Variation_Name	GeneID	GeneSymbol	ClinicalSignificance	dbSNP	RCVaccession	TestedInGTR	PhenotypeIDs	Chromosome	Start	Stop	HGVS_c	HGVS_p	HGVS_g	OtherIDs	Disease_ClinVar
NM_004595.4(SMS):c.166G>A (p.Gly56Ser)	6611	SMS	Pathogenic	121434610	RCV000012390; RCV000210586;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063; MedGen:C0950123	X	21985430	21985430	NM_004595.4:c.166G>A	NP_004586.2:p.Gly56Ser	NC_000023.10:g.21985430G>A	OMIM Allelic Variant:300105.0002	C0950123 Inborn genetic diseases; C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.174T>A (p.Phe58Leu)	6611	SMS	Pathogenic	397515549	RCV000055902;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21990018	21990018	NM_004595.4:c.174T>A	NP_004586.2:p.Phe58Leu	NC_000023.10:g.21990018T>A	-	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.200G>A (p.Gly67Glu)	6611	SMS	Pathogenic	397515550	RCV000055903;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21990044	21990044	NM_004595.4:c.200G>A	NP_004586.2:p.Gly67Glu	NC_000023.10:g.21990044G>A	OMIM Allelic Variant:300105.0005	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.329+5G>A	6611	SMS	Pathogenic	397515381	RCV000012389;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21990694	21990694	NM_004595.4:c.329+5G>A		NC_000023.10:g.21990694G>A	OMIM Allelic Variant:300105.0001	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.395T>G (p.Val132Gly)	6611	SMS	Pathogenic	267607076	RCV000012391;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21995244	21995244	NM_004595.4:c.395T>G	NP_004586.2:p.Val132Gly	NC_000023.10:g.21995244T>G	OMIM Allelic Variant:300105.0003	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.443A>G (p.Gln148Arg)	6611	SMS	Pathogenic	397515551	RCV000055905;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21995292	21995292	NM_004595.4:c.443A>G	NP_004586.2:p.Gln148Arg	NC_000023.10:g.21995292A>G	-	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.449T>C (p.Ile150Thr)	6611	SMS	Pathogenic	397515552	RCV000055906;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	21995298	21995298	NM_004595.4:c.449T>C	NP_004586.2:p.Ile150Thr	NC_000023.10:g.21995298T>C	-	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.983A>C (p.Tyr328Ser)	6611	SMS	Pathogenic	397515553	RCV000055907;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	22010752	22010752	NM_004595.4:c.983A>C	NP_004586.2:p.Tyr328Ser	NC_000023.10:g.22010752A>C,NC_000023.10:g.22010752A>G	-	C0796160 309583 Snyder Robinson syndrome
NM_004595.4(SMS):c.983A>G (p.Tyr328Cys)	6611	SMS	Pathogenic	397515553	RCV000074415;	N	MedGen:C0796160,OMIM:309583,ORPHA:3063	X	22010752	22010752	NM_004595.4:c.983A>G	NP_004586.2:p.Tyr328Cys	NC_000023.10:g.22010752A>C,NC_000023.10:g.22010752A>G	OMIM Allelic Variant:300105.0004	C0796160 309583 Snyder Robinson syndrome