Absent speech
Symptom Information:
Symptom ID: | HPO:0001344 | |||||||||
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) Absent speech(HPO:0001344) Cognitive impairment(HPO:0100543) Delayed speech and language development(HPO:0000750) Absent speech(HPO:0001344) MedDRA: |
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Database Frequency: | 57 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
ALG11-CDG | (Orphanet:280071) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Angelman syndrome | (Orphanet:72) |
Autosomal recessive spastic paraplegia type 18 | (Orphanet:209951) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
COG4-CDG | (Orphanet:263501) |
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 | (OMIM:615282) |
Cabezas syndrome | (Orphanet:85293) |
Christianson syndrome | (Orphanet:85278) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Congenital cataract-hearing loss-severe developmental delay syndrome | (Orphanet:300313) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 | (OMIM:615473) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 | (OMIM:616139) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 | (OMIM:616341) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE | (OMIM:240000) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Intellectual deficit - alacrima - achalasia | (Orphanet:289483) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Joubert syndrome 20 | (OMIM:614970) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MEGDEL syndrome | (Orphanet:352328) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 | (OMIM:616078) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 | (OMIM:616158) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49 | (OMIM:616281) |
MENTAL RETARDATION, X-LINKED 101 | (OMIM:300928) |
MENTAL RETARDATION, X-LINKED 91 | (OMIM:300577) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4 | (OMIM:615159) |
MPDU1-CDG | (Orphanet:79323) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14 | (OMIM:615350) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 | (OMIM:615351) |
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type | (Orphanet:217026) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mucolipidosis type 4 | (Orphanet:578) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
OPTICOCOCHLEODENTATE DEGENERATION | (OMIM:258700) |
OROFACIODIGITAL SYNDROME XIV | (OMIM:615948) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 | (OMIM:615803) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Transketolase deficiency | (ORPHA:488618) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | (Orphanet:324410) |