Concept information
Preferred term
Hereditary disorder of endocrine systen
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Beckwith-Wiedemann syndrome
- Congenital adrenal hyperplasia
- Congenital isolated adrenocorticotropic hormone deficiency (disorder)
- Congenital pancreatic enterokinase deficiency
- Diabetes mellitus AND insipidus with optic atrophy AND deafness
- Dyshormonogenic goitre
- Familial adrenocortical hypoplasia
- Hereditary adrenal unresponsiveness to corticotropin
- Hereditary breast and ovarian cancer syndrome (disorder)
- Hereditary infantile gigantism
- Hereditary nephrogenic diabetes insipidus
- Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome (disorder)
- Inherited disorder of thyroid metabolism
- Kallman syndrome with heart disease (disorder)
- Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
- Moderate steroid 21-hydroxylase deficiency
- Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder)
- Multiple endocrine neoplasia, type 1
- Multiple endocrine neoplasia, type 2
- Multiple endocrine neoplasia, type 3
- Pancreatic colipase deficiency
- Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)
- Pancreatic triacylglycerol lipase deficiency
- Polyglandular autoimmune syndrome, type 1
- Pseudohypoaldosteronism, type 1, dominant form
- Pseudohypoaldosteronism, type 1, recessive form
- Pseudohypoparathyroidism type I A
- Severe steroid 21-hydroxylase deficiency
- Shwachman syndrome
- Sotos' syndrome
Finding site
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/363104002
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}