Mental retardation, mild-moderate

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Mental retardation, mild-moderate (28%, usually in males) [OMIM:Mental retardation, mild-moderate (28%, usually in males)]
Mental retardation, mild-moderate (some) [OMIM:Mental retardation, mild-moderate (some)]
Mild-moderate mental retardation [OMIM:Mild-moderate mental retardation]
Mild-moderate mental retardation (80% affected males) [OMIM:Mild-moderate mental retardation (80% affected males)]
Quality:
Cross references:
OMIM: "Mental retardation, mild-moderate" [OMIM:Mental retardation, mild-moderate]
OMIM: "Mental retardation, mild-moderate (28%, usually in males)" [OMIM:Mental retardation, mild-moderate (28%, usually in males)]
OMIM: "Mental retardation, mild-moderate (some)" [OMIM:Mental retardation, mild-moderate (some)]
OMIM: "Mild-moderate mental retardation" [OMIM:Mild-moderate mental retardation]
OMIM: "Mild-moderate mental retardation (80% affected males)" [OMIM:Mild-moderate mental retardation (80% affected males)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microduplication syndrome (Orphanet:250994)
MENTAL RETARDATION, X-LINKED 93 (OMIM:300659)
Nance-Horan syndrome (Orphanet:627)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Richieri Costa-da Silva syndrome (Orphanet:3101)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)