The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Hypophosphatasia
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Hypophosphatasia 6 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypophosphatasia 6 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
Annotation: | defic of blood phosphatases; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
historyNote*: | 72(66)
X |
publicMeSHNote*: | 72
X |
Scope note: | A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin D-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (From Dorland, 27th ed)
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1972-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Hypofosfatasia (fi) XHypofosfatasemia (fi, replaced) Hypophosphatasia (la-FI, replaced) |
Share: |
Loading results...