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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
7 associated genes
No signs/symptoms info
Hypomyelination with atrophy of basal ganglia and cerebellum
Hereditary pheochromocytoma-paraganglioma

TUBB4A MAX
SDHA
SDHAF2
SDHB
SDHC
SDHD
TMEM127


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TUBB4A
(0.49)
MAX



Citations in the biomedical literature:


Hypomyelination with atrophy of basal ganglia and cerebellum
TUBB4A
Hereditary pheochromocytoma-paraganglioma
MAX SDHA SDHAF2 SDHB SDHC SDHD
TMEM127



Hypomyelination with atrophy of basal ganglia and cerebellum
Hereditary pheochromocytoma-paraganglioma

Synonym(s):
- H-ABC

Synonym(s):
- Familial pheochromocytoma-paraganglioma
- SDHx-related paraganglioma-pheochromocytoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references

No signs/symptoms info available.