Intellectual disability, mild

Basic details

Preferred term: Intellectual disability, mild
Alt. terms: Intellectual disability, mild | Mental retardation, borderline-mild | Mental retardation, mild | Mild and nonprogressive mental retardation | Mild mental retardation

HPO term: Intellectual disability, mild
HPO code: HP:0001256

GenIA ID: 1773
Last updated on: 2021-08-02 21:50:33

Cross ref. with other ontologies

NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -

Description

Mild intellectual disability is defined as an intelligence quotient (IQ) in the range of 50-69.

Hierarchical classification

TERM

Intellectual disability, mild

CHILD terms

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101884 M 212237tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.A:III.3(A.II.3)]
101962 M 212237tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.A:III.2(A.II.2)]
101975 F 214053tree icon - Turkish Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.D:IV.2(D.II.1)]; PMID:34390440 [HIES53]; PMID:31980991 [Case]
102124 F 214351tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.B:IV.5(B.II.4)]
102129 F 214351tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.B:IV.1(B.II.1)]
102133 M 214352tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.C:II.1(C.II.1)]
102134 M 214352tree icon - Sudanese Intellectual disability Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.C:II.6(C.II.6)]
102313 M 214935tree icon - Turkish Intellectual disability Otofaciocervical syndrome 2 PMID:23851939 [V-2(V.2)]
102353 M 214936tree icon - Indian Intellectual disability Otofaciocervical syndrome 2 PMID:29681087 [P1(II.1)]
102356 F 214936tree icon - Indian Intellectual disability Otofaciocervical syndrome 2 PMID:29681087 [Fam.P1:II.2(P2)]
102950 M 215049 - Italian Intellectual disability T-cell lymphopenia with or without nail dystrophy, AD PMID:31447097 [P41]; PMID:37419334 [P41(22)]
103116 F 215101tree icon - Saudi Intellectual disability Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [P1(IV.4)]
103128 F 215101tree icon - Saudi Intellectual disability Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.5]
103129 F 215101tree icon - Saudi Intellectual disability Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.6]
103131 M 215101tree icon - Saudi Intellectual disability Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.8]
103859 M 215263tree icon - Turkish Intellectual disability Adenosine deaminase 2 deficiency PMID:24552284 [Fam.8:II.1(P9)]; PMID:26233953 [Fam.F4:P5]
104698 M 215571tree icon - Iranian Intellectual disability Cohen syndrome PMID:37382373 [Fam.1:V.1]
104709 F 215571tree icon - Iranian Intellectual disability Cohen syndrome PMID:37382373 [Fam.1:VI.1]
104710 M 215571tree icon - Iranian Intellectual disability Cohen syndrome PMID:37382373 [Fam.1:VI.2]
105261 F 215680 - Egyptian Intellectual disability Otofaciocervical syndrome 2 PMID:37924468 [Patient(III.1)]
106047 F 215930 - Caucasian Intellectual disability CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.LL:II.1(LL.II.1 (86))]
106079 M 215935 - Intellectual disability 4q24 deletion syndrome PMID:150198 [Fam.EI:586]; PMID:35784294 [1580]
106080 F 215936 - Intellectual disability 4q24 deletion syndrome PMID:150198 [Fam.EJ:587]; PMID:35784294 [249234]
106082 F 215938 - Intellectual disability 4q24 deletion syndrome PMID:150198 [Fam.EL:589]; PMID:35784294 [263047]
106654 M 216101tree icon - Syrian Intellectual disability Intellectual disability due to EZR deficiency PMID:25504542 [Fam.MR037:IV.1(IV-1)]
106667 M 216101tree icon - Syrian Intellectual disability Intellectual disability due to EZR deficiency PMID:25504542 [Fam.MR037:IV.3(IV-3)]

*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).