Poor speech
Symptom Information:
Symptom ID: | HPO:0002465 | ||
Synonyms: |
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Quality: | |||
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) Poor speech(HPO:0002465) MedDRA: |
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Database Frequency: | 31 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
Cystic leukoencephalopathy without megalencephaly | (Orphanet:85136) |
Dysequilibrium syndrome | (Orphanet:1766) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypomyelination with atrophy of basal ganglia and cerebellum | (Orphanet:139441) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Koolen-De Vries syndrome | (Orphanet:96169) |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS | (OMIM:613671) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27 | (OMIM:614340) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40 | (OMIM:615599) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 | (OMIM:616116) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47 | (OMIM:616193) |
MENTAL RETARDATION, X-LINKED 100 | (OMIM:300923) |
MENTAL RETARDATION, X-LINKED 101 | (OMIM:300928) |
MENTAL RETARDATION, X-LINKED 14 | (OMIM:300062) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 | (OMIM:615824) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
MYASTHENIC SYNDROME, CONGENITAL, 18 | (OMIM:616330) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 | (OMIM:616204) |