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Autosomal recessive limb-girdle muscular dystrophy type 2P
1 OMIM reference -
1 associated gene
32 connected diseases
No signs/symptoms info
Disease Type of connection
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
Familial isolated dilated cardiomyopathy
Postsynaptic congenital myasthenic syndromes
Congenital muscular dystrophy type 1A
Becker muscular dystrophy
Duchenne muscular dystrophy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Romano-Ward syndrome
Fetal akinesia deformation sequence
Lethal multiple pterygium syndrome
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Lissencephaly due to TUBA1A mutation
Autosomal dominant macrothrombocytopenia
Autosomal recessive limb-girdle muscular dystrophy type 2D
Charcot-Marie-Tooth disease type 4F
Dejerine-Sottas syndrome
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal agammaglobulinemia
Autosomal dominant Larsen syndrome
Behavioral variant of frontotemporal dementia
Boomerang dysplasia
Early-onset autosomal dominant Alzheimer disease
Progressive non-fluent aphasia
SHORT syndrome
Semantic dementia
Spondylocarpotarsal synostosis

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
DAG1 Q14118128239
No signs/symptoms info available.