Poor speech

Symptom Information:

Symptom ID: HPO:0002465
Synonyms:
Poor speech [OMIM:Poor speech]
Quality:
Cross references:
OMIM: "Poor speech" [OMIM:Poor speech]
Is a (Direct Parents):
HPO         Neurological speech 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)
                Neurological speech impairment(HPO:0002167)
                   Poor speech(HPO:0002465)
MedDRA:
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)