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Nestor-Guillermo progeria syndrome
1 OMIM reference -
1 associated gene
52 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
X-linked Emery-Dreifuss muscular dystrophy
Cone rod dystrophy
Leber congenital amaurosis
Retinitis pigmentosa
Acrofacial dysostosis, Weyers type
Acute promyelocytic leukemia
Ataxia - oculomotor apraxia type 1
Atypical Werner syndrome
Atypical dentin dysplasia due to SMOC2 deficiency
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
Autosomal recessive distal renal tubular acidosis with deafness
Charcot-Marie-Tooth disease type 2B1
Chronic intestinal pseudoobstruction
Coffin-Siris syndrome
Combined oxidative phosphorylation defect type 4
Congenital muscular dystrophy due to LMNA mutation
Congenital short bowel syndrome
Congenital valvular dysplasia
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Ehlers-Danlos syndrome with periventricular heterotopia
Ellis Van Creveld syndrome
Epidermolytic palmoplantar keratoderma
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 multiple meningioma
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Frontometaphyseal dysplasia
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
Intellectual deficit - sparse hair - brachydactyly
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachyonychia congenita
Partial acquired lipodystrophy
Periventricular nodular heterotopia
Progeria-associated arthropathy
Terminal osseous dysplasia - pigmentary defects
Xeroderma pigmentosum complementation group C
Xeroderma pigmentosum complementation group E

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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
BANF1 O75531603811
No signs/symptoms info available.