Specific learning disability

Symptom Information:

Symptom ID: HPO:0001328
Synonyms:
Learning disability [Orphanet:43510]
Learning disorder [Orphanet:43510]
Learning difficulties (finding) [Orphanet:43510]
Learning difficulties [Orphanet:43510]
Learning Disorders [Orphanet:43510]
Learning Disabilities [Orphanet:43510]
Intellectual deficit/mental/psychomotor retardation/learning disability [Orphanet:43510]
Learning disorder [MedDRA:10061265]
Learning disorder NOS [MedDRA:10061265]
Other specific developmental learning difficulties [MedDRA:10061265]
Other specific learning delay [MedDRA:10061265]
Specific learning delay (excl mental retardation) [MedDRA:10061265]
Learning disability [MedDRA:10024092]
Learning difficulties [OMIM:Learning difficulties]
Learning difficulties (classic feature) [OMIM:Learning difficulties (classic feature)]
Learning difficulties (in some patients) [OMIM:Learning difficulties (in some patients)]
Learning difficulties (less common) [OMIM:Learning difficulties (less common)]
Learning difficulties (seen in recessive form) [OMIM:Learning difficulties (seen in recessive form)]
Learning disabilities [OMIM:Learning disabilities]
Learning disabilities (1 family) [OMIM:Learning disabilities (1 family)]
Learning disabilities (in females) [OMIM:Learning disabilities (in females)]
Learning disabilities (in some patients) [OMIM:Learning disabilities (in some patients)]
Learning disabilities (in some) [OMIM:Learning disabilities (in some)]
Learning disabilities (major) [OMIM:Learning disabilities (major)]
Learning disability [OMIM:Learning disability]
Learning disability (90% patients) [OMIM:Learning disability (90% patients)]
Learning disability (early in life) [OMIM:Learning disability (early in life)]
Learning disability (in some patients) [OMIM:Learning disability (in some patients)]
Learning disorders [MedDRA:10024094]
Quality:
Cross references:
Orphanet:43510 "Intellectual deficit/mental/psychomotor retardation/learning disability" [Orphanet:43510]
OMIM: "Learning difficulties" [OMIM:Learning difficulties]
OMIM: "Learning difficulties (classic feature)" [OMIM:Learning difficulties (classic feature)]
OMIM: "Learning difficulties (in some patients)" [OMIM:Learning difficulties (in some patients)]
OMIM: "Learning difficulties (less common)" [OMIM:Learning difficulties (less common)]
OMIM: "Learning difficulties (seen in recessive form)" [OMIM:Learning difficulties (seen in recessive form)]
OMIM: "Learning disabilities" [OMIM:Learning disabilities]
OMIM: "Learning disabilities (1 family)" [OMIM:Learning disabilities (1 family)]
OMIM: "Learning disabilities (in females)" [OMIM:Learning disabilities (in females)]
OMIM: "Learning disabilities (in some patients)" [OMIM:Learning disabilities (in some patients)]
OMIM: "Learning disabilities (in some)" [OMIM:Learning disabilities (in some)]
OMIM: "Learning disabilities (major)" [OMIM:Learning disabilities (major)]
OMIM: "Learning disability" [OMIM:Learning disability]
OMIM: "Learning disability (90% patients)" [OMIM:Learning disability (90% patients)]
OMIM: "Learning disability (early in life)" [OMIM:Learning disability (early in life)]
OMIM: "Learning disability (in some patients)" [OMIM:Learning disability (in some patients)]
UMLS:C0424939 "Learning difficulties" [Orphanet:43510]
UMLS:C0023186 "Learning Disorders" [Orphanet:43510]
UMLS:C0751265 "Learning Disabilities" [Orphanet:43510]
Is a (Direct Parents):
MedDRA Cognitive and attention disorders and disturbances
MedDRA Disability issues
Orphanet Functional anomalies of the nervous system
Orphanet Intellectual disability
HPO         Cognitive impairment
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)
                   Specific learning disability(HPO:0001328)
MedDRA:
Social circumstances(MedDRA:10041244)
    Lifestyle issues(MedDRA:10024450)
       Disability issues(MedDRA:10057171)
          Specific learning disability(HPO:0001328)
Database Frequency: 114 / 7739
Resource:

All diseases associated with this symptom:

15q13.3 microdeletion syndrome (Orphanet:199318)
17q11.2 microduplication syndrome (Orphanet:139474)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
22q11.2 microduplication syndrome (Orphanet:1727)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 3 (Orphanet:67047)
3-methylglutaconic aciduria type 4 (Orphanet:67048)
48,XXYY syndrome (Orphanet:10)
Acromegaloid facial appearance syndrome (Orphanet:965)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alström syndrome (Orphanet:64)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Autosomal dominant Charcot-Marie-Tooth disease type 2O (Orphanet:284232)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Autosomal recessive spastic ataxia - optic atrophy - dysarthria (Orphanet:254343)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Barth syndrome (Orphanet:111)
Behr syndrome (Orphanet:1239)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bilateral frontal polymicrogyria (Orphanet:208444)
Bloom syndrome (Orphanet:125)
Brain calcification, Rajab type (Orphanet:178506)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Classical phenylketonuria (Orphanet:79254)
Congenital heart block (Orphanet:60041)
Constitutional megaloblastic anemia with severe neurologic disease (Orphanet:319651)
Cystinosis (Orphanet:213)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Delayed speech - facial asymmetry - strabismus - ear lobe creases (Orphanet:3038)
Dihydropteridine reductase deficiency (Orphanet:226)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 6p (Orphanet:96125)
Dyskeratosis congenita (Orphanet:1775)
Encephalopathy due to GLUT1 deficiency (Orphanet:71277)
Epileptic encephalopathy with continuous spike-and-wave during sleep (Orphanet:725)
FEINGOLD SYNDROME 1 (OMIM:164280)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
FRAXE intellectual deficit (Orphanet:100973)
Familial lambdoid synostosis (Orphanet:3267)
Feingold syndrome (Orphanet:1305)
GIACHETI SYNDROME (OMIM:612917)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Hypomyelination with atrophy of basal ganglia and cerebellum (Orphanet:139441)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit, X-linked, Shashi type (Orphanet:85286)
Isolated plagiocephaly (Orphanet:35098)
Landau-Kleffner syndrome (Orphanet:98818)
Legius syndrome (Orphanet:137605)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
Lymphangioleiomyomatosis (Orphanet:538)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA (OMIM:608624)
MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600)
MUSICAL PERFECT PITCH (OMIM:159300)
MYOPATHY WITH EXTRAPYRAMIDAL SIGNS (OMIM:615673)
Maple syrup urine disease (Orphanet:511)
Menkes disease (Orphanet:565)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Moebius syndrome (Orphanet:570)
Mowat-Wilson syndrome (Orphanet:2152)
Mucolipidosis type 3 (Orphanet:577)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Niemann-Pick disease type C (Orphanet:646)
Noonan syndrome with multiple lentigines (Orphanet:500)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Partial acquired lipodystrophy (Orphanet:79087)
Polymicrogyria due to TUBB2B mutation (Orphanet:300573)
Prader-Willi syndrome (Orphanet:739)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Renal cysts and diabetes syndrome (Orphanet:93111)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Shwachman-Diamond syndrome (Orphanet:811)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Steinert myotonic dystrophy (Orphanet:273)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tuberous sclerosis (Orphanet:805)
Tyrosinemia type 2 (Orphanet:28378)
Tyrosinemia type 3 (Orphanet:69723)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Wilson-Turner syndrome (Orphanet:3459)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked epilepsy - learning disabilities - behavior disorders (Orphanet:85294)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
X-linked mandibulofacial dysostosis (Orphanet:1131)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Xq27.3q28 duplication syndrome (Orphanet:261483)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)