Diko : en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland

en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland

Catégories

Nom

Informations lexicales

Langue:anglais

Liens externes

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umls:CL515340

Associations d'idées

[F]

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111

en:primary pigmented nodular adrenocortical disease

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en:leukotriene c4 synthase deficiency

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en:glutamate dehydrogenase 1 hyperinsulinism

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en:familial thyroid dyshormonogenesis

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en:hyperparathyroidism-jaw tumor syndrome

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en:autosomal dominant hypoparathyroidism

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en:martsolf syndrome

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en:sohval soffer syndrome

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en:secondary hypoparathyroidism

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en:feigenbaum bergeron richardson syndrome

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en:hypogonadism-cataract syndrome

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en:iatrogenic hypoparathyroidism

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en:bamforth syndrome

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en:hyperinsulinism due to hnf4a deficiency

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en:hypoparathyroidism following procedure

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en:multiple endocrine neoplasia type 1

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en:beckwith-wiedemann syndrome

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en:hereditary glucocorticoid resistance

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en:moloney syndrome

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en:sotos' syndrome

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en:teebi naguib al awadi syndrome

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en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome

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en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome

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en:glucocorticoid deficiency with achalasia

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en:pseudohypoaldosteronism, type 1, recessive form

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en:isolated late onset hypoparathyroidism

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en:x-linked intellectual disability with acromegaly and hyperactivity syndrome

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en:simpson-golabi-behmel syndrome

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en:congenital adrenal hyperplasia

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en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome

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en:insulin-dependent diabetes mellitus secretory diarrhea syndrome

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en:primary hypoparathyroidism

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en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism

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en:adrenoleukodystrophy

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en:autosomal dominant hyperinsulinism due to sur1 deficiency

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en:combined pituitary hormone deficiency genetic form

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en:inherited disorder of thyroid metabolism

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en:hydrocephalus with obesity and hypogonadism syndrome

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en:moderate steroid 21-hydroxylase deficiency

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en:hypoparathyroidism - x-linked

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en:familial hypoaldosteronism

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en:hereditary vitamin d dependency syndrome

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en:idiopathic parathyroidism

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en:pituitary adenoma, familial isolated (disorder)

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en:multiple endocrine neoplasia type 2b

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en:heterozygous methylenetetrahydrofolate reductase mutation

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en:pseudohypoparathyroidism

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en:autosomal recessive hypoparathyroidism

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en:transient neonatal hypoparathyroidism

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en:deafness-hypogonadism syndrome

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en:hypoparathyroidism due to granulomatous disease

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en:3-hydroxyacyl-coa dehydrogenase deficiency

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en:homozygous methylenetetrahydrofolate reductase mutation

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en:hypoparathyroidism due to hemochromatosis

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en:familial adrenocortical hypoplasia

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en:digeorge syndrome

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en:short stature, pituitary and cerebellar defect and small sella turcica syndrome

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en:paraganglioma and gastric stromal sarcoma

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en:hyperinsulinism due to hnf1a deficiency

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en:hypogonadism with prune belly syndrome

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en:transient hypoparathyroidism

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en:other hypoparathyroidism

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en:hypoparathyroidism, idiopathic

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en:acquired hypoparathyroidism

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en:dahlberg borer newcomer syndrome

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en:hereditary adrenal unresponsiveness to corticotropin

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en:hyperinsulinism due to deficiency of glucokinase

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en:hypothyroidism due to mutation in transcription factor of pituitary development

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en:liddle syndrome

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en:parathyroid hypocalcemic tetany

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en:wnt4 mullerian aplasia and ovarian dysfunction

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en:yorifuji okuno syndrome

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en:22q11 deletion syndrome

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en:adrenal gland hyperplasia ii

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en:hyperinsulinemic hypoglycemia, familial, 7

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en:hyperinsulinism due to insulin receptor deficiency

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en:sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome

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en:x-linked adrenal hypoplasia congenita

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en:tetany

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en:autoimmune hypoparathyroidism

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en:hereditary isolated hypoparathyroidism due to impaired parathormone secretion

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en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome

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en:scholte syndrome

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en:autosomal dominant hyperinsulinism due to kir6.2 deficiency

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en:mental retardation, x-linked, syndromic 7

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en:najjar syndrome

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en:x-linked intellectual disability van esch type

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en:x-linked intellectual disability with precocious puberty and obesity syndrome

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en:kallmann syndrome

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en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome

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en:familial non-autoimmune autosomal dominant hyperthyroidism

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en:hypoparathyroidism due to impaired pth secretion

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en:congenital hypoparathyroidism

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en:combined d-2- and l-2-hydroxyglutaric aciduria

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en:hypomagnesemia 1, intestinal

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en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome

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en:pseudohypoaldosteronism, type 1, dominant form

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en:schaap taylor baraitser syndrome

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en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism

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en:hyperinsulinism due to uncoupling protein 2 deficiency

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en:neonatal hypoparathyroidism

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en:x-linked intellectual disability cilliers type

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en:congenital nephrogenic diabetes insipidus

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en:multiple endocrine neoplasia type 2a

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en:severe steroid 21-hydroxylase deficiency

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en:hereditary

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adréno-leucodystrophie

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hypogonadisme avec anosmie

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dysplasie olfacto-génitale

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dysplasie olfactogénitale de De Morsier

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en:disease or syndrome

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