Mental retardation, moderate to severe

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Mental retardation, moderate to severe (10-15% of patients) [OMIM:Mental retardation, moderate to severe (10-15% of patients)]
Mental retardation, moderate to severe (IQ 40 to 60) [OMIM:Mental retardation, moderate to severe (IQ 40 to 60)]
Mental retardation, moderate to severe (in some patients) [OMIM:Mental retardation, moderate to severe (in some patients)]
Mental retardation, moderate to severe (type II, infantile and juvenile) [OMIM:Mental retardation, moderate to severe (type II, infantile and juvenile)]
Quality:
Cross references:
OMIM: "Mental retardation, moderate to severe" [OMIM:Mental retardation, moderate to severe]
OMIM: "Mental retardation, moderate to severe (10-15% of patients)" [OMIM:Mental retardation, moderate to severe (10-15% of patients)]
OMIM: "Mental retardation, moderate to severe (IQ 40 to 60)" [OMIM:Mental retardation, moderate to severe (IQ 40 to 60)]
OMIM: "Mental retardation, moderate to severe (in some patients)" [OMIM:Mental retardation, moderate to severe (in some patients)]
OMIM: "Mental retardation, moderate to severe (type II, infantile and juvenile)" [OMIM:Mental retardation, moderate to severe (type II, infantile and juvenile)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

ANE syndrome (Orphanet:157954)
Atkin-Flaitz syndrome (Orphanet:1193)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
Bilateral generalized polymicrogyria (Orphanet:208447)
CLARK-BARAITSER SYNDROME (OMIM:300602)
Dubowitz syndrome (Orphanet:235)
Hypomyelination with atrophy of basal ganglia and cerebellum (Orphanet:139441)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 (OMIM:613192)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 31 (OMIM:614329)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 (OMIM:615541)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
Monosomy 22q13 (Orphanet:48652)
Mowat-Wilson syndrome (Orphanet:2152)
Recombinant 8 syndrome (Orphanet:96167)
Sialidosis type 1 (Orphanet:812)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
X-linked intellectual deficit, Najm type (Orphanet:163937)