Lack of speech development
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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| Lack of speech development (45%) [OMIM:Lack of speech development (45%)] | | Lack of speech development (some patients) [OMIM:Lack of speech development (some patients)] |
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Quality:
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Cross references:
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| OMIM: "Lack of speech development" [OMIM:Lack of speech development] | | OMIM: "Lack of speech development (45%)" [OMIM:Lack of speech development (45%)] | | OMIM: "Lack of speech development (some patients)" [OMIM:Lack of speech development (some patients)] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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20 / 7739
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Resource:
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All diseases associated with this symptom:
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5q14.3 microdeletion syndrome
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(Orphanet:228384)
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Amelo-cerebro-hypohidrotic syndrome
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(Orphanet:1946)
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Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome
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(Orphanet:363429)
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Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
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(Orphanet:324262)
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CEREBROOCULOFACIOSKELETAL SYNDROME 1
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(OMIM:214150)
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Cabezas syndrome
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(Orphanet:85293)
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DDOST-CDG
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(Orphanet:300536)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14
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(OMIM:614959)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15
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(OMIM:615006)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
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(OMIM:300672)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5
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(OMIM:613477)
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Intellectual deficit - alacrima - achalasia
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(Orphanet:289483)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2
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(OMIM:613156)
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PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM
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(OMIM:614501)
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RETT SYNDROME, CONGENITAL VARIANT
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(OMIM:613454)
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SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE
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(OMIM:612936)
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SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
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(OMIM:613744)
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SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
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(OMIM:614067)
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TMCO1 defect syndrome
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(Orphanet:228407)
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X-linked intellectual deficit, Najm type
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(Orphanet:163937)
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