Intellectual disability, mild

Symptom Information:

Symptom ID: HPO:0001256
Synonyms:
Mental retardation, borderline-mild [HPO:0001256]
Mental retardation, mild [HPO:0001256]
Mild and nonprogressive mental retardation [HPO:0001256]
Mild mental retardation [HPO:0001256]
Intellectual disability, mild [OMIM:Intellectual disability, mild]
Mental retardation, borderline-mild [OMIM:Mental retardation, borderline-mild]
Mental retardation, mild [OMIM:Mental retardation, mild]
Mild and nonprogressive mental retardation [OMIM:Mild and nonprogressive mental retardation]
Mild mental retardation [OMIM:Mild mental retardation]
Intellectual disability, mild (in some patients) [OMIM:Intellectual disability, mild (in some patients)]
Intellectual disability, mild (uncommon) [OMIM:Intellectual disability, mild (uncommon)]
Mental retardation, mild (1 family) [OMIM:Mental retardation, mild (1 family)]
Mental retardation, mild (1 patient) [OMIM:Mental retardation, mild (1 patient)]
Mental retardation, mild (11%) [OMIM:Mental retardation, mild (11%)]
Mental retardation, mild (18%) [OMIM:Mental retardation, mild (18%)]
Mental retardation, mild (2 families) [OMIM:Mental retardation, mild (2 families)]
Mental retardation, mild (20% have more severe mental retardation) [OMIM:Mental retardation, mild (20% have more severe mental retardation)]
Mental retardation, mild (IQ range from 50 to 70) [OMIM:Mental retardation, mild (IQ range from 50 to 70)]
Mental retardation, mild (carrier females) [OMIM:Mental retardation, mild (carrier females)]
Mental retardation, mild (in some females) [OMIM:Mental retardation, mild (in some females)]
Mental retardation, mild (in some patients) [OMIM:Mental retardation, mild (in some patients)]
Mental retardation, mild (in some) [OMIM:Mental retardation, mild (in some)]
Mental retardation, mild (rare) [OMIM:Mental retardation, mild (rare)]
Mental retardation, mild, (in some patients) [OMIM:Mental retardation, mild, (in some patients)]
Mild mental retardation (in 1/4 patients) [OMIM:Mild mental retardation (in 1/4 patients)]
Mild mental retardation (some) [OMIM:Mild mental retardation (some)]
Mild mental retardation [MedDRA:10027618]
Quality:
Cross references:
OMIM: "Intellectual disability, mild" [OMIM:Intellectual disability, mild]
OMIM: "Mental retardation, borderline-mild" [OMIM:Mental retardation, borderline-mild]
OMIM: "Mental retardation, mild" [OMIM:Mental retardation, mild]
OMIM: "Mild and nonprogressive mental retardation" [OMIM:Mild and nonprogressive mental retardation]
OMIM: "Mild mental retardation" [OMIM:Mild mental retardation]
OMIM: "Intellectual disability, mild (in some patients)" [OMIM:Intellectual disability, mild (in some patients)]
OMIM: "Intellectual disability, mild (uncommon)" [OMIM:Intellectual disability, mild (uncommon)]
OMIM: "Mental retardation, mild (1 family)" [OMIM:Mental retardation, mild (1 family)]
OMIM: "Mental retardation, mild (1 patient)" [OMIM:Mental retardation, mild (1 patient)]
OMIM: "Mental retardation, mild (11%)" [OMIM:Mental retardation, mild (11%)]
OMIM: "Mental retardation, mild (18%)" [OMIM:Mental retardation, mild (18%)]
OMIM: "Mental retardation, mild (2 families)" [OMIM:Mental retardation, mild (2 families)]
OMIM: "Mental retardation, mild (20% have more severe mental retardation)" [OMIM:Mental retardation, mild (20% have more severe mental retardation)]
OMIM: "Mental retardation, mild (IQ range from 50 to 70)" [OMIM:Mental retardation, mild (IQ range from 50 to 70)]
OMIM: "Mental retardation, mild (carrier females)" [OMIM:Mental retardation, mild (carrier females)]
OMIM: "Mental retardation, mild (in some females)" [OMIM:Mental retardation, mild (in some females)]
OMIM: "Mental retardation, mild (in some patients)" [OMIM:Mental retardation, mild (in some patients)]
OMIM: "Mental retardation, mild (in some)" [OMIM:Mental retardation, mild (in some)]
OMIM: "Mental retardation, mild (rare)" [OMIM:Mental retardation, mild (rare)]
OMIM: "Mental retardation, mild, (in some patients)" [OMIM:Mental retardation, mild, (in some patients)]
OMIM: "Mild mental retardation (in 1/4 patients)" [OMIM:Mild mental retardation (in 1/4 patients)]
OMIM: "Mild mental retardation (some)" [OMIM:Mild mental retardation (some)]
Is a (Direct Parents):
HPO         Intellectual disability
MedDRA Intellectual disability
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Cognitive impairment(HPO:0100543)
                   Intellectual disability(HPO:0001249)
                      Intellectual disability, mild(HPO:0001256)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Mental impairment disorders(MedDRA:10057167)
       Intellectual disability(HPO:0001249)
          Intellectual disability, mild(HPO:0001256)
Social circumstances(MedDRA:10041244)
    Lifestyle issues(MedDRA:10024450)
       Disability issues(MedDRA:10057171)
          Intellectual disability(HPO:0001249)
             Intellectual disability, mild(HPO:0001256)
Database Frequency: 141 / 7739
Resource:

All diseases associated with this symptom:

15q13.3 microdeletion syndrome (Orphanet:199318)
16p13.3 microduplication syndrome (Orphanet:96078)
17p11.2 microduplication syndrome (Orphanet:1713)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
1q21.1 microduplication syndrome (Orphanet:250994)
2-aminoadipic 2-oxoadipic aciduria (Orphanet:79154)
3MC SYNDROME 1 (OMIM:257920)
AUROCEPHALOSYNDACTYLY (OMIM:109050)
Acromegaloid facial appearance syndrome (Orphanet:965)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alopecia - intellectual deficit - hypergonadotropic hypogonadism (Orphanet:1014)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Atkin-Flaitz syndrome (Orphanet:1193)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb-girdle muscular dystrophy type 2T (Orphanet:363623)
Autosomal recessive spastic paraplegia type 14 (Orphanet:100995)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
Autosomal recessive spastic paraplegia type 32 (Orphanet:171622)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 19 (OMIM:615996)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bloom syndrome (Orphanet:125)
Bonnemann-Meinecke-Reich syndrome (Orphanet:1261)
Branchio-oculo-facial syndrome (Orphanet:1297)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CANDLE syndrome (Orphanet:325004)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3 (OMIM:613227)
CHILD syndrome (Orphanet:139)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24 (OMIM:616239)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Cat-eye syndrome (Orphanet:195)
Cataract - ataxia - deafness (Orphanet:1368)
Char syndrome (Orphanet:46627)
Chudley-McCullough syndrome (Orphanet:314597)
Cowden syndrome (Orphanet:201)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Darier disease (Orphanet:218)
Deafness - encephaloneuropathy - obesity - valvulopathy (Orphanet:254898)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Duchenne muscular dystrophy (Orphanet:98896)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Ermine phenotype (Orphanet:999)
FRONTOOCULAR SYNDROME (OMIM:605321)
Familial vascular leukoencephalopathy (Orphanet:36383)
GM1 gangliosidosis type 3 (Orphanet:79257)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3 (OMIM:614207)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
HYPERTELORISM AND TETRALOGY OF FALLOT (OMIM:239711)
HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA (OMIM:614839)
Hemihypertrophy (Orphanet:2128)
Hereditary sensory and autonomic neuropathy type 5 (Orphanet:64752)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypomyelination with brain stem and spinal cord involvement and leg spasticity (Orphanet:363412)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated growth hormone deficiency type III (Orphanet:231692)
JMP syndrome (Orphanet:324999)
Keutel syndrome (Orphanet:85202)
LEOPARD SYNDROME 1 (OMIM:151100)
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM (OMIM:614381)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Leigh syndrome (Orphanet:506)
Lesch-Nyhan syndrome (Orphanet:510)
Lowry-Wood syndrome (Orphanet:1824)
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1 (OMIM:604004)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2 (OMIM:607417)
MENTAL RETARDATION, X-LINKED 49 (OMIM:300114)
MENTAL RETARDATION, X-LINKED 50 (OMIM:300115)
MENTAL RETARDATION, X-LINKED 58 (OMIM:300210)
MENTAL RETARDATION, X-LINKED 73 (OMIM:300355)
MENTAL RETARDATION, X-LINKED 9 (OMIM:309549)
MENTAL RETARDATION, X-LINKED 91 (OMIM:300577)
MENTAL RETARDATION, X-LINKED 93 (OMIM:300659)
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION (OMIM:249670)
MONOAMINE OXIDASE A (OMIM:309850)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
McKusick-Kaufman syndrome (Orphanet:2473)
Megalencephalic leukoencephalopathy with subcortical cysts (Orphanet:2478)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Mietens syndrome (Orphanet:2557)
Moebius syndrome (Orphanet:570)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mulibrey nanism (Orphanet:2576)
NOONAN SYNDROME 6 (OMIM:613224)
Nakajo-Nishimura syndrome (Orphanet:2615)
Nephronophthisis 15 (OMIM:614845)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Nodular neuronal heterotopia (Orphanet:2149)
Non-progressive cerebellar ataxia with intellectual deficit (Orphanet:314647)
Noonan syndrome with multiple lentigines (Orphanet:500)
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA (OMIM:258360)
OTOFACIOCERVICAL SYNDROME 1 (OMIM:166780)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteoporosis - pseudoglioma (Orphanet:2788)
Otofaciocervical syndrome (Orphanet:2792)
Otopalatodigital syndrome type 1 (Orphanet:90650)
PEROXISOME BIOGENESIS DISORDER 14B (OMIM:614920)
PGM1-CDG (Orphanet:319646)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Proteasome disability syndrome (Orphanet:324977)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Pyruvate dehydrogenase deficiency (Orphanet:765)
ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED (OMIM:300643)
Richieri Costa-da Silva syndrome (Orphanet:3101)
Roifman syndrome (Orphanet:353298)
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency (Orphanet:353284)
Schilbach-Rott syndrome (Orphanet:2353)
Senior-Loken syndrome 7 (OMIM:613615)
Shwachman-Diamond syndrome (Orphanet:811)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spinocerebellar ataxia type 27 (Orphanet:98764)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)
Temtamy syndrome (Orphanet:1777)
Tyrosinemia type 3 (Orphanet:69723)
VAN BOGAERT-HOZAY SYNDROME (OMIM:277150)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
XFE PROGEROID SYNDROME (OMIM:610965)
Xq27.3q28 duplication syndrome (Orphanet:261483)