H disease - meaning and definition. What is H disease
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What (who) is H disease - definition

SPECIES OF MYXOSPOREA
Henneguya salminicola; Henneguya salminocola; H. zschokkei; H. salminicola; Tapioca disease

Hemoglobin H disease         
ALPHA THALASSEMIA THAT HAS MATERIAL BASIS IN CONTIGUOUS GENE DELETION OF THE HEMOGLOBIN ALPHA-1 (HBA1) AND ALPHA-2 (HBA2) GENES ON ONE CHROMOSOME 16, AND A DEFECT, DELETIONAL OR NONDELETIONAL, IN EITHER HBA1 OR HBA2 ON THE OTHER
Hemoglobin H
Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.
Kimura's disease         
HUMAN DISEASE
Kimura´s disease; Kimura disease
Kimura's disease is a benign rare chronic inflammatory disorder. Its primary symptoms are subdermal lesions in the head or neck or painless unilateral inflammation of cervical lymph nodes.
Bright's disease         
HISTORICAL CLASSIFICATION OF NEPHRITIS
Bright's Disease; Brights Disease; Blight's Disease; Bright disease; Bright's (renal) disease
·- An affection of the kidneys, usually inflammatory in character, and distinguished by the occurrence of albumin and renal casts in the urine. Several varieties of Bright's disease are now recognized, differing in the part of the kidney involved, and in the intensity and course of the morbid process.

Wikipedia

Henneguya zschokkei

Henneguya zschokkei or Henneguya salminicola is a species of a myxosporean endoparasite. It afflicts several salmon in the genus Oncorhynchus. It causes milky flesh or tapioca disease. H. zschokkei is notable for its absence of mitochondria, mitochondrial DNA, aerobic respiration and its reliance on an as of yet undiscovered energy metabolism.