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Autosomal dominant limb-girdle muscular dystrophy type 1D
1 OMIM reference -
1 associated gene
70 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
2q37 microdeletion syndrome
Burkitt lymphoma
Cerebellar ataxia - hypogonadism
Muscular dystrophy, Selcen type
Precursor T-cell acute lymphoblastic leukemia
ADULT syndrome
Adrenocortical carcinoma
Alternating hemiplegia of childhood
Amyotrophic lateral sclerosis
Ankyloblepharon - ectodermal defects - cleft lip / palate
Anophthalmia / microphthalmia - esophageal atresia
Autosomal recessive centronuclear myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy type 2J
B-cell chronic lymphocytic leukemia
Bladder exstrophy
CLOVE syndrome
Colobomatous microphthalmia
Congenital myopathy, Paradas type
Cowden syndrome
Digitotalar dysmorphism
Distal myopathy with anterior tibial onset
EEC syndrome
Early infantile epileptic encephalopathy
Early-onset myopathy with fatal cardiomyopathy
Essential thrombocythemia
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial or sporadic hemiplegic migraine
Familial pancreatic carcinoma
Fanconi anemia
Frontotemporal dementia with motor neuron disease
Giant cell glioblastoma
Gliosarcoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Glycogen storage disease due to phosphoglucomutase deficiency
Hemimegalencephaly
Hereditary nonpolyposis colon cancer
Hereditary proximal myopathy with early respiratory failure
Isolated anophthalmia - microphthalmia
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
Lethal congenital contracture syndrome type 3
Li-Fraumeni syndrome
Limb-mammary syndrome
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Miyoshi myopathy
PGM-CDG
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Pseudohypoaldosteronism type 2E
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Septo-optic dysplasia
Short stature due to growth hormone qualitative anomaly
Split hand-split foot malformation
Tibial muscular dystrophy
Treacher-Collins syndrome
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
- LGMD1D

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: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
DNAJB6 O75190611332
No signs/symptoms info available.