Loss of speech

Symptom Information:

Symptom ID: HPO:0002371
Synonyms:
Loss of speech [OMIM:Loss of speech]
Loss of speech (1 patient) [OMIM:Loss of speech (1 patient)]
Quality:
Cross references:
OMIM: "Loss of speech" [OMIM:Loss of speech]
OMIM: "Loss of speech (1 patient)" [OMIM:Loss of speech (1 patient)]
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)
                   Loss of speech(HPO:0002371)
MedDRA:
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)