Mental retardation, mild to profound
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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Quality:
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Cross references:
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| OMIM: "Mental retardation, mild to profound" [OMIM:Mental retardation, mild to profound] |
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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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3 / 7739
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Resource:
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All diseases associated with this symptom:
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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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Macrocephaly - spastic paraplegia - dysmorphism
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(Orphanet:2429)
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