Cognitive impairment, mild

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Cognitive impairment, mild (1 patient) [OMIM:Cognitive impairment, mild (1 patient)]
Cognitive impairment, mild (44%) [OMIM:Cognitive impairment, mild (44%)]
Cognitive impairment, mild (in 2 of 3 patients) [OMIM:Cognitive impairment, mild (in 2 of 3 patients)]
Mild cognitive impairment (in 2 patients) [OMIM:Mild cognitive impairment (in 2 patients)]
Mild cognitive impairment (in some patients) [OMIM:Mild cognitive impairment (in some patients)]
Mild cognitive impairment (less common) [OMIM:Mild cognitive impairment (less common)]
Quality:
Cross references:
OMIM: "Cognitive impairment, mild" [OMIM:Cognitive impairment, mild]
OMIM: "Cognitive impairment, mild (1 patient)" [OMIM:Cognitive impairment, mild (1 patient)]
OMIM: "Cognitive impairment, mild (44%)" [OMIM:Cognitive impairment, mild (44%)]
OMIM: "Cognitive impairment, mild (in 2 of 3 patients)" [OMIM:Cognitive impairment, mild (in 2 of 3 patients)]
OMIM: "Mild cognitive impairment (in 2 patients)" [OMIM:Mild cognitive impairment (in 2 patients)]
OMIM: "Mild cognitive impairment (in some patients)" [OMIM:Mild cognitive impairment (in some patients)]
OMIM: "Mild cognitive impairment (less common)" [OMIM:Mild cognitive impairment (less common)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic ataxia with leukoencephalopathy (Orphanet:314603)
Autosomal recessive spastic paraplegia type 23 (Orphanet:101003)
Autosomal recessive spastic paraplegia type 44 (Orphanet:320401)
Congenital myopathy with internal nuclei and atypical cores (Orphanet:319160)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Joubert syndrome 4 (OMIM:609583)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5 (OMIM:615160)
Multiple system atrophy (Orphanet:102)
NOONAN SYNDROME 4 (OMIM:610733)
Progressive myoclonic epilepsy type 6 (Orphanet:280620)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 29 (Orphanet:208513)
Spinocerebellar ataxia type 5 (Orphanet:98766)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)