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Acute necrotizing encephalopathy of childhood
1 OMIM reference -
2 associated genes
86 connected diseases
No signs/symptoms info
Disease Type of connection
Carnitine palmitoyl transferase II deficiency, myopathic form
Carnitine palmitoyl transferase II deficiency, neonatal form
Carnitine palmitoyl transferase II deficiency, severe infantile form
Familial acute necrotizing encephalopathy
Inflammatory myofibroblastic tumor
Young adult-onset Parkinsonism
Desmoid tumor
Blue cone monochromatism
Cone rod dystrophy
Precursor T-cell acute lymphoblastic leukemia
APC-related attenuated familial adenomatous polyposis
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Turcot syndrome with polyposis
Burkitt lymphoma
Congenital analbuminemia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Hyperparathyroidism - jaw tumor syndrome
Parathyroid carcinoma
17q11 microdeletion syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute promyelocytic leukemia
Autoimmune polyendocrinopathy type 1
Autosomal dominant nonsyndromic intellectual deficit
Familial isolated dilated cardiomyopathy
Hepatocellular carcinoma, childhood-onset
Inherited acute myeloid leukemia
Jeune syndrome
Muscular dystrophy, Selcen type
Rare isolated myopia
Saldino-Mainzer syndrome
X-linked dystonia-parkinsonism
2q37 microdeletion syndrome
Catecholaminergic polymorphic ventricular tachycardia
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Dedifferentiated liposarcoma
Essential thrombocythemia
Familial infantile bilateral striatal necrosis
Familial pancreatic carcinoma
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Well-differentiated liposarcoma
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Chronic intestinal pseudoobstruction
Congenital muscular dystrophy due to LMNA mutation
Congenital short bowel syndrome
Congenital valvular dysplasia
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Distal myopathy with vocal cord weakness
Ehlers-Danlos syndrome with periventricular heterotopia
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Frontometaphyseal dysplasia
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Progeria-associated arthropathy
Severe combined immunodeficiency due to DNA-PKcs deficiency
Terminal osseous dysplasia - pigmentary defects
- Isolated ANE
- Isolated acute necrotizing encephalopathy

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
CPT2 P23786600650
RANBP2 P49792601181
No signs/symptoms info available.