Intellectual disability, moderate

Symptom Information:

Symptom ID: HPO:0002342
Synonyms:
Mental retardation, moderate [HPO:0002342]
Moderate mental deficiency [HPO:0002342]
Moderate mental retardation [HPO:0002342]
Intellectual disability, moderate [OMIM:Intellectual disability, moderate]
Mental retardation, moderate [OMIM:Mental retardation, moderate]
Moderate mental deficiency [OMIM:Moderate mental deficiency]
Moderate mental retardation [OMIM:Moderate mental retardation]
Intellectual disability, moderate (in some patients) [OMIM:Intellectual disability, moderate (in some patients)]
Mental retardation, moderate (apparent by age 4 years) [OMIM:Mental retardation, moderate (apparent by age 4 years)]
Mental retardation, moderate (in 1 patient) [OMIM:Mental retardation, moderate (in 1 patient)]
Mental retardation, moderate (in some patients) [OMIM:Mental retardation, moderate (in some patients)]
Moderate mental retardation [MedDRA:10027791]
Quality:
Cross references:
OMIM: "Intellectual disability, moderate" [OMIM:Intellectual disability, moderate]
OMIM: "Mental retardation, moderate" [OMIM:Mental retardation, moderate]
OMIM: "Moderate mental deficiency" [OMIM:Moderate mental deficiency]
OMIM: "Moderate mental retardation" [OMIM:Moderate mental retardation]
OMIM: "Intellectual disability, moderate (in some patients)" [OMIM:Intellectual disability, moderate (in some patients)]
OMIM: "Mental retardation, moderate (apparent by age 4 years)" [OMIM:Mental retardation, moderate (apparent by age 4 years)]
OMIM: "Mental retardation, moderate (in 1 patient)" [OMIM:Mental retardation, moderate (in 1 patient)]
OMIM: "Mental retardation, moderate (in some patients)" [OMIM:Mental retardation, moderate (in some patients)]
Is a (Direct Parents):
HPO         Intellectual disability
MedDRA Intellectual disability
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)
                Cognitive impairment(HPO:0100543)
                   Intellectual disability(HPO:0001249)
                      Intellectual disability, moderate(HPO:0002342)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Mental impairment disorders(MedDRA:10057167)
       Intellectual disability(HPO:0001249)
          Intellectual disability, moderate(HPO:0002342)
Social circumstances(MedDRA:10041244)
    Lifestyle issues(MedDRA:10024450)
       Disability issues(MedDRA:10057171)
          Intellectual disability(HPO:0001249)
             Intellectual disability, moderate(HPO:0002342)
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

15q13.3 microdeletion syndrome (Orphanet:199318)
Acro-pectoral syndrome (Orphanet:85203)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bilateral generalized polymicrogyria (Orphanet:208447)
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation (Orphanet:300570)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Familial primary hypomagnesemia with normocalcuria and normocalcemia (Orphanet:34527)
Fragile X syndrome (Orphanet:908)
Intellectual deficiency - hypotonia - spasticity - sleep disorder (Orphanet:356996)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Intellectual deficit, X-linked - cubitus valgus - dysmorphism (Orphanet:85280)
Intellectual deficit, X-linked - plagiocephaly (Orphanet:2898)
Intellectual deficit, X-linked, Shashi type (Orphanet:85286)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Joubert syndrome with hepatic defect (Orphanet:1454)
Leigh syndrome (Orphanet:506)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lesch-Nyhan syndrome (Orphanet:510)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 (OMIM:614202)
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENISSYNDROME (OMIM:610156)
MENTAL RETARDATION, X-LINKED 14 (OMIM:300062)
MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:604804)
MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:608393)
MICROPHTHALMIA, SYNDROMIC 14 (OMIM:615877)
Monosomy 22q13 (Orphanet:48652)
Mowat-Wilson syndrome (Orphanet:2152)
Nance-Horan syndrome (Orphanet:627)
OTOFACIOCERVICAL SYNDROME 2 (OMIM:615560)
PACHYGYRIA, FRONTOTEMPORAL (OMIM:610279)
Proteus syndrome (Orphanet:744)
Saethre-Chotzen syndrome (Orphanet:794)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked intellectual deficit, Najm type (Orphanet:163937)