Loss of speech
Symptom Information:
Symptom ID: | HPO:0002371 | ||
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) Loss of speech(HPO:0002371) MedDRA: |
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Database Frequency: | 15 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 6 | (OMIM:615010) |
Adrenomyeloneuropathy | (Orphanet:139399) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
CLN1 disease | (Orphanet:228329) |
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency | (Orphanet:293955) |
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY | (OMIM:615924) |
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE | (OMIM:615889) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
NIEMANN-PICK DISEASE, TYPE C1 | (OMIM:257220) |
NIEMANN-PICK DISEASE, TYPE C2 | (OMIM:607625) |
Sanfilippo syndrome type C | (Orphanet:79271) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |