Intellectual disability, mild
Symptom Information:
Symptom ID: | HPO:0001256 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |