Specific learning disability
Symptom Information:
Symptom ID: | HPO:0001328 | |||||||||||||||||||||||||||||
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) Specific learning disability(HPO:0001328) MedDRA: Social circumstances(MedDRA:10041244) Lifestyle issues(MedDRA:10024450) Disability issues(MedDRA:10057171) Specific learning disability(HPO:0001328) |
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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) |