ODCs

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4 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
22 signs/symptoms

Hereditary spherocytosis

Osteopetrosis with renal tubular acidosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC4A1	(0.86)	CA2

Citations in the biomedical literature:

Hereditary spherocytosis		Osteopetrosis with renal tubular acidosis
	Synonym(s): - Minkowski-Chauffard disease		Synonym(s): - Carbonic anhydrase 2 deficiency - Guibaud-Vainsel syndrome - Marble brain disease - Mixed RTA - Mixed renal tubular acidosis - Renal tubular acidosis type 3

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 4 OMIM references - 2 MeSH references: C536356 / D013103		External references: 2 OMIM references - 1 MeSH reference: C536058

Osteopetrosis with renal tubular acidosis
	Very frequent - Anaemia - Autosomal recessive inheritance - Bone pain - Epiphyseal anomaly - Failure to thrive / difficulties for feeding in infancy / growth delay - Genu valgum - Hepatomegaly / liver enlargement (excluding storage disease) - Intellectual deficit / mental / psychomotor retardation / learning disability - Mutiple fractures / bone fragility - Osteonecrosis / bone infarction - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets - Osteosclerosis / osteopetrosis / bone condensation - Renal tubular defect / tubulopathy - Splenomegaly Frequent - Intracranial / cerebral calcifications - Multiple caries - Peripheral neuropathy - Prognathism / prognathia - Thrombocytopenia / thrombopenia - Tooth shape anomaly Occasional - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Visual loss / blindness / amblyopia
Hereditary spherocytosis
(no data available)