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Congenital muscular dystrophy with intellectual disability
5 OMIM references -
5 associated genes
34 connected diseases
No signs/symptoms info
Disease Type of connection
Muscle-eye-brain disease
Congenital muscular dystrophy with cerebellar involvement
Walker-Warburg syndrome
Congenital muscular dystrophy without intellectual disability
Autosomal recessive limb-girdle muscular dystrophy type 2K
Autosomal recessive limb-girdle muscular dystrophy type 2N
Autosomal recessive limb-girdle muscular dystrophy type 2I
Autosomal recessive limb-girdle muscular dystrophy type 2T
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Triple A syndrome
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal acantholytic epidermolysis bullosa
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Naxos disease
Progeria-associated arthropathy
Synonym(s):
- CMD with intellectual disability
- CMD-MR

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
External references:
5 OMIM references -
No MeSH references

No signs/symptoms info available.