Mental retardation, mild to severe
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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| Mild to severe mental retardation (24%) [OMIM:Mild to severe mental retardation (24%)] | | Mild-to-severe mental retardation [OMIM:Mild-to-severe mental retardation] |
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Quality:
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Cross references:
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| OMIM: "Mental retardation, mild to severe" [OMIM:Mental retardation, mild to severe] | | OMIM: "Mild to severe mental retardation (24%)" [OMIM:Mild to severe mental retardation (24%)] | | OMIM: "Mild-to-severe mental retardation" [OMIM:Mild-to-severe mental retardation] |
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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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14 / 7739
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Resource:
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All diseases associated with this symptom:
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Bannayan-Riley-Ruvalcaba syndrome
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(Orphanet:109)
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Corpus callosum agenesis - neuronopathy
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(Orphanet:1496)
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Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
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(Orphanet:300570)
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Deafness - intellectual deficit, Martin-Probst type
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(Orphanet:85321)
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Hyperprolinemia type 1
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(Orphanet:419)
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Koolen-De Vries syndrome
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(Orphanet:96169)
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MENTAL RETARDATION, AUTOSOMAL DOMINANT 5
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(OMIM:612621)
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MENTAL RETARDATION, X-LINKED 30
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(OMIM:300558)
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MENTAL RETARDATION, X-LINKED, SYNDROMIC 14
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(OMIM:300676)
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MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE
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(OMIM:608716)
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MICROPHTHALMIA, SYNDROMIC 7
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(OMIM:309801)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14
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(OMIM:615351)
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Premature chromosome condensation with microcephaly and intellectual deficit
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(Orphanet:52183)
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Wiedemann-Rautenstrauch syndrome
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(Orphanet:3455)
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