Intellectual disability, moderate
Symptom Information:
Symptom ID: | HPO:0002342 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |