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
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101884 | M | 212237![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.A:III.3(A.II.3)] |
101962 | M | 212237![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.A:III.2(A.II.2)] |
101975 | F | 214053![]() |
- | 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 | 214351![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.B:IV.5(B.II.4)] |
102129 | F | 214351![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.B:IV.1(B.II.1)] |
102133 | M | 214352![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.C:II.1(C.II.1)] |
102134 | M | 214352![]() |
- | Sudanese | Intellectual disability | Hyper-IgE recurrent infection syndrome 3 | PMID:29907690 [Fam.C:II.6(C.II.6)] |
102313 | M | 214935![]() |
- | Turkish | Intellectual disability | Otofaciocervical syndrome 2 | PMID:23851939 [V-2(V.2)] |
102353 | M | 214936![]() |
- | Indian | Intellectual disability | Otofaciocervical syndrome 2 | PMID:29681087 [P1(II.1)] |
102356 | F | 214936![]() |
- | 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 | 215101![]() |
- | Saudi | Intellectual disability | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [P1(IV.4)] |
103128 | F | 215101![]() |
- | Saudi | Intellectual disability | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.5] |
103129 | F | 215101![]() |
- | Saudi | Intellectual disability | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.6] |
103131 | M | 215101![]() |
- | Saudi | Intellectual disability | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.8] |
103859 | M | 215263![]() |
- | Turkish | Intellectual disability | Adenosine deaminase 2 deficiency | PMID:24552284 [Fam.8:II.1(P9)]; PMID:26233953 [Fam.F4:P5] |
104698 | M | 215571![]() |
- | Iranian | Intellectual disability | Cohen syndrome | PMID:37382373 [Fam.1:V.1] |
104709 | F | 215571![]() |
- | Iranian | Intellectual disability | Cohen syndrome | PMID:37382373 [Fam.1:VI.1] |
104710 | M | 215571![]() |
- | 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 | 216101![]() |
- | Syrian | Intellectual disability | Intellectual disability due to EZR deficiency | PMID:25504542 [Fam.MR037:IV.1(IV-1)] |
106667 | M | 216101![]() |
- | 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).