Neurological speech impairment
Symptom Information:
Symptom ID: | HPO:0002167 | |||||||||
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) Neurological speech impairment(HPO:0002167) MedDRA: |
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Database Frequency: | 308 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
10q22.3q23.3 microduplication syndrome | (Orphanet:276422) |
12q14 microdeletion syndrome | (Orphanet:94063) |
14q12 microdeletion syndrome | (Orphanet:261144) |
15q11q13 microduplication syndrome | (Orphanet:238446) |
15q14 microdeletion syndrome | (Orphanet:261190) |
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
16p11.2p12.2 microduplication syndrome | (Orphanet:261204) |
16p13.11 microduplication syndrome | (Orphanet:261243) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
17q12 microdeletion syndrome | (Orphanet:261265) |
17q12 microduplication syndrome | (Orphanet:261272) |
17q21.31 microduplication syndrome | (Orphanet:217340) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
1p36 deletion syndrome | (Orphanet:1606) |
1q44 microdeletion syndrome | (Orphanet:238769) |
22q11.2 deletion syndrome | (Orphanet:567) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2p21 microdeletion syndrome | (Orphanet:163693) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
3C syndrome | (Orphanet:7) |
3q29 microdeletion syndrome | (Orphanet:65286) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
4q21 microdeletion syndrome | (Orphanet:238750) |
5q14.3 microdeletion syndrome | (Orphanet:228384) |
6q16 deletion syndrome | (Orphanet:171829) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
8p23.1 microduplication syndrome | (Orphanet:251076) |
ALZHEIMER DISEASE 10 | (OMIM:609636) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Aceruloplasminemia | (Orphanet:48818) |
Achondroplasia | (Orphanet:15) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acromesomelic dysplasia, Hunter-Thomson type | (Orphanet:968) |
Acroosteolysis, dominant type | (Orphanet:955) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Albinism-deafness syndrome | (Orphanet:998) |
Alexander disease | (Orphanet:58) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alopecia antibody deficiency | (Orphanet:1006) |
Alpha-mannosidosis | (Orphanet:61) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Alveolar echinococcosis | (Orphanet:284) |
Angelman syndrome | (Orphanet:72) |
Aniridia - cerebellar ataxia - intellectual deficit | (Orphanet:1065) |
Argininemia | (Orphanet:90) |
Aspartylglucosaminuria | (Orphanet:93) |
Ataxia - pancytopenia | (Orphanet:2585) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Ataxia-telangiectasia | (Orphanet:100) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
Autosomal recessive cerebelloparenchymal disorder type 3 | (Orphanet:1170) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Benign familial infantile seizures | (Orphanet:306) |
Beta-mannosidosis | (Orphanet:118) |
Beta-ureidopropionase deficiency | (Orphanet:65287) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Botulism | (Orphanet:1267) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CADASIL | (Orphanet:136) |
CAMOS syndrome | (Orphanet:83472) |
CHARGE syndrome | (Orphanet:138) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Cabezas syndrome | (Orphanet:85293) |
Camurati-Engelmann disease | (Orphanet:1328) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Central bilateral macrogyria | (Orphanet:2431) |
Central congenital hypothyroidism | (Orphanet:226298) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Cerebro-reno-digital syndrome | (Orphanet:1396) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Choreoacanthocytosis | (Orphanet:2388) |
Christianson syndrome | (Orphanet:85278) |
Classic galactosemia | (Orphanet:79239) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cogan syndrome | (Orphanet:1467) |
Cohen syndrome | (Orphanet:193) |
Congenital rubella syndrome | (Orphanet:290) |
Cornelia de Lange syndrome | (Orphanet:199) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Cystinosis | (Orphanet:213) |
DYSLEXIA, SUSCEPTIBILITY TO, 1 | (OMIM:127700) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Deafness - epiphyseal dysplasia - short stature | (Orphanet:3218) |
Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Delayed speech - facial asymmetry - strabismus - ear lobe creases | (Orphanet:3038) |
Dermatomyositis | (Orphanet:221) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal 7q11.23 microduplication syndrome | (Orphanet:261102) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Ectodermal dysplasia - blindness | (Orphanet:1806) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Erdheim-Chester disease | (Orphanet:35687) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Familial developmental dysphasia | (Orphanet:1799) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Familial thrombocytosis | (Orphanet:71493) |
Filippi syndrome | (Orphanet:3255) |
Floating-Harbor syndrome | (Orphanet:2044) |
Flynn-Aird syndrome | (Orphanet:2047) |
Foodborne botulism | (Orphanet:228371) |
Fountain syndrome | (Orphanet:3219) |
Fragile X syndrome | (Orphanet:908) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Free sialic acid storage disease | (Orphanet:834) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Fried syndrome | (Orphanet:85335) |
Fumaric aciduria | (Orphanet:24) |
GIACHETI SYNDROME | (OMIM:612917) |
Galactosemia | (Orphanet:352) |
Gaucher disease type 3 | (Orphanet:77261) |
Genitopatellar syndrome | (Orphanet:85201) |
German syndrome | (Orphanet:2077) |
Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Goldenhar syndrome | (Orphanet:374) |
Good syndrome | (Orphanet:169105) |
HERNS syndrome | (Orphanet:63261) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Histidinemia | (Orphanet:2157) |
Huntington disease-like 3 | (Orphanet:157946) |
Hypertrichosis cubiti - short stature | (Orphanet:2220) |
Hypertryptophanemia | (Orphanet:2224) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
Ichthyosis - hepatosplenomegaly - cerebellar degeneration | (Orphanet:2274) |
Infant botulism | (Orphanet:178478) |
Infantile axonal neuropathy | (Orphanet:2679) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
Intellectual deficit, X-linked, Pai type | (Orphanet:85322) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Intestinal botulism | (Orphanet:178481) |
Isolated cerebellar hypoplasia/agenesis | (Orphanet:1398) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile dermatomyositis | (Orphanet:93672) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Kallmann syndrome | (Orphanet:478) |
Kennedy disease | (Orphanet:481) |
Kleefstra syndrome | (Orphanet:261494) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Koolen-De Vries syndrome | (Orphanet:96169) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
L1 syndrome | (Orphanet:275543) |
Locked-in syndrome | (Orphanet:2406) |
Low birth weight - dwarfism - dysgammaglobulinemia | (Orphanet:2621) |
MASA syndrome | (Orphanet:2466) |
MELAS | (Orphanet:550) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Metachromatic leukodystrophy | (Orphanet:512) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Microphthalmia, Lenz type | (Orphanet:568) |
Mietens syndrome | (Orphanet:2557) |
Mild Canavan disease | (Orphanet:314918) |
Monosomy 22q13 | (Orphanet:48652) |
Mucolipidosis type 4 | (Orphanet:578) |
Muscle-eye-brain disease | (Orphanet:588) |
Muscular pseudohypertrophy - hypothyroidism | (Orphanet:2349) |
Myoclonus - cerebellar ataxia - deafness | (Orphanet:2589) |
Nager syndrome | (Orphanet:245) |
Narcolepsy-cataplexy | (Orphanet:2073) |
Nasu-Hakola disease | (Orphanet:2770) |
Neuhauser-Eichner-Opitz syndrome | (Orphanet:2672) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurodegeneration with brain iron accumulation | (Orphanet:385) |
Neuroferritinopathy | (Orphanet:157846) |
Neurofibromatosis type 1 | (Orphanet:636) |
Neurofibromatosis type 2 | (Orphanet:637) |
Neuronal ceroid lipofuscinosis | (Orphanet:216) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
Niemann-Pick disease type C | (Orphanet:646) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Noonan syndrome | (Orphanet:648) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Olivopontocerebellar atrophy - deafness | (Orphanet:2732) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otofaciocervical syndrome | (Orphanet:2792) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Pelizaeus-Merzbacher disease | (Orphanet:702) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Pendred syndrome | (Orphanet:705) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Phosphoribosylpyrophosphate synthetase superactivity | (Orphanet:3222) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Polymyositis | (Orphanet:732) |
Posterior cortical atrophy | (Orphanet:54247) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Pseudoprogeria syndrome | (Orphanet:2985) |
Psychogenic movement disorders | (Orphanet:71519) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Recessive X-linked ichthyosis | (Orphanet:461) |
Refsum disease | (Orphanet:773) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Rett syndrome | (Orphanet:778) |
Rheumatic fever | (Orphanet:3099) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SHORT syndrome | (Orphanet:3163) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Sialidosis type 1 | (Orphanet:812) |
Sialidosis type 2 | (Orphanet:87876) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Smith-Magenis syndrome | (Orphanet:819) |
Sneddon syndrome | (Orphanet:820) |
Spastic ataxia with congenital miosis | (Orphanet:1182) |
Spastic paraplegia - facial-cutaneous lesions | (Orphanet:2819) |
Spastic paraplegia - nephritis - deafness | (Orphanet:2820) |
Spastic paraplegia - precocious puberty | (Orphanet:2826) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Sturge-Weber syndrome | (Orphanet:3205) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
Syndromic X-linked intellectual deficit 7 | (Orphanet:85274) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Takayasu arteritis | (Orphanet:3287) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Thymic tumor | (Orphanet:100100) |
Toluene embryopathy | (Orphanet:1920) |
Treacher-Collins syndrome | (Orphanet:861) |
Trisomy 13 | (Orphanet:3378) |
Trisomy 20p | (Orphanet:261318) |
Trisomy Xq28 | (Orphanet:1762) |
Tyrosinemia type 2 | (Orphanet:28378) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Von Hippel-Lindau disease | (Orphanet:892) |
Weaver-Williams syndrome | (Orphanet:3448) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolfram syndrome | (Orphanet:3463) |
Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |
Worster-Drought syndrome | (Orphanet:3465) |
Wound botulism | (Orphanet:178475) |
Wyburn-Mason syndrome | (Orphanet:53719) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |