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Disease association ontology term - MONDO:0005151 - endocrine system disorder

Term summary

ID
MONDO:0005151
Name
endocrine system disorder
Ontology or CV name
Disease association
Definition
A disease involving the endocrine system.

Parents

Annotation

Disease association

MONDO:0009299 - 46 XX gonadal dysgenesis

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MONDO:0009916 - 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency

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MONDO:8000015 - 46,XY sex reversal 11

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MONDO:0700299 - ACTH-independent macronodular adrenal hyperplasia 3

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MONDO:0013111 - acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

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MONDO:0008294 - acute intermittent porphyria

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MONDO:0012794 - ANE syndrome

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MONDO:0009025 - apparent mineralocorticoid excess

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MONDO:0008840 - ataxia telangiectasia

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MONDO:0008980 - ataxia-hypogonadism-choroidal dystrophy syndrome

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MONDO:0000447 - autosomal dominant polycystic liver disease

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MONDO:0011559 - benign recurrent intrahepatic cholestasis type 2

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MONDO:0011365 - blepharophimosis - intellectual disability syndrome, SBBYS type

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MONDO:0011740 - Carney-Stratakis syndrome

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MONDO:0014455 - cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

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MONDO:0019165 - central precocious puberty

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MONDO:0013995 - cholestasis, intrahepatic, of pregnancy, 3

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MONDO:0030810 - cholestasis, progressive familial intrahepatic, 10

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MONDO:0031040 - cholestasis, progressive familial intrahepatic, 12

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MONDO:0010814 - chondrodysplasia-pseudohermaphroditism syndrome

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MONDO:0009258 - classic galactosemia

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MONDO:0013310 - congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency

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MONDO:0011503 - cortisone reductase deficiency 1

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MONDO:0009050 - Cushing disease due to pituitary adenoma

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MONDO:0005015 - diabetes mellitus

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MONDO:0014488 - diabetes mellitus, noninsulin-dependent, 5

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MONDO:0958224 - encephalopathy, porphyria-related

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MONDO:0001676 - erythropoietic protoporphyria

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MONDO:0010926 - familial hypocalciuric hypercalcemia 3

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MONDO:0015278 - familial pancreatic carcinoma

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MONDO:0008296 - familial porphyria cutanea tarda

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MONDO:0005032 - follicular thyroid adenoma

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MONDO:0007681 - goiter, multinodular 1, with or without Sertoli-Leydig cell tumors

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MONDO:0005364 - Graves disease

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MONDO:0002520 - hepatic porphyria

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MONDO:0007256 - hepatocellular carcinoma

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MONDO:0007369 - hereditary coproporphyria

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MONDO:0032787 - holoprosencephaly 12 with or without pancreatic agenesis

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MONDO:0026763 - holoprosencephaly 13, X-linked

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MONDO:0030886 - holoprosencephaly 14

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MONDO:0005803 - hyperinsulinemic hypoglycemia

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MONDO:0011236 - hyperinsulinemic hypoglycemia, familial, 3

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MONDO:0859362 - hyperinsulinemic hypoglycemia, familial, 8

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MONDO:0011717 - hyperinsulinism-hyperammonemia syndrome

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MONDO:0007767 - hyperparathyroidism 1

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MONDO:0007768 - hyperparathyroidism 2 with jaw tumors

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MONDO:0007785 - hyperthyroxinemia, dystransthyretinemic

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MONDO:0009416 - hypoinsulinemic hypoglycemia and body hemihypertrophy

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MONDO:0013722 - hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism

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MONDO:0026731 - hypothyroidism, congenital, nongoitrous, 8

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MONDO:0015713 - idiopathic central precocious puberty

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MONDO:0024568 - infantile liver failure syndrome 1

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MONDO:0014659 - infantile liver failure syndrome 2

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MONDO:0032844 - infantile liver failure syndrome 3

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MONDO:0009514 - Laurence-Moon syndrome

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MONDO:0958226 - leukoencephalopathy, porphyria-related

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MONDO:0024477 - liver and intrahepatic bile duct neoplasm

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MONDO:0018911 - maturity-onset diabetes of the young

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MONDO:0014674 - maturity-onset diabetes of the young type 14

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MONDO:0007453 - maturity-onset diabetes of the young type 2

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MONDO:0015967 - monogenic diabetes

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MONDO:0016391 - neonatal diabetes mellitus

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MONDO:0010961 - obesity due to prohormone convertase I deficiency

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MONDO:0008170 - ovarian cancer

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MONDO:0030736 - ovarian dysgenesis 10

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MONDO:0013689 - ovarian dysgenesis 3

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MONDO:0054850 - ovarian dysgenesis 6

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MONDO:0012992 - pancreatic insufficiency-anemia-hyperostosis syndrome

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MONDO:0000448 - paraganglioma

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MONDO:0012004 - parathyroid gland carcinoma

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MONDO:0010134 - Pendred syndrome

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MONDO:0100165 - permanent neonatal diabetes mellitus 1

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MONDO:0017312 - Perrault syndrome

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MONDO:0013972 - Perrault syndrome 2

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MONDO:0014126 - Perrault syndrome 4

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MONDO:0976232 - Perrault syndrome 7

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MONDO:0008192 - pheochromocytoma/paraganglioma syndrome 1

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MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2

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MONDO:0011544 - pheochromocytoma/paraganglioma syndrome 3

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MONDO:0007273 - pheochromocytoma/paraganglioma syndrome 4

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MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5

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MONDO:0032771 - pheochromocytoma/paraganglioma syndrome 7

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MONDO:0014359 - pigmented nodular adrenocortical disease, primary, 4

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MONDO:0008265 - polycystic liver disease 1

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MONDO:0014860 - polycystic liver disease 2

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MONDO:0054743 - polycystic liver disease 3 with or without kidney cysts

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MONDO:0014497 - polyendocrine-polyneuropathy syndrome

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MONDO:0015104 - porphyria cutanea tarda

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MONDO:0013000 - porphyria due to ALA dehydratase deficiency

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MONDO:0014843 - premature ovarian failure 11

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MONDO:0054862 - premature ovarian failure 15

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MONDO:0030870 - premature ovarian failure 17

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MONDO:0958035 - premature ovarian failure 23

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MONDO:0010350 - premature ovarian failure 2A

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MONDO:0014321 - premature ovarian failure 8

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MONDO:0010837 - primary hyperparathyroidism

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MONDO:0011156 - progressive familial intrahepatic cholestasis type 2

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MONDO:0011214 - progressive familial intrahepatic cholestasis type 3

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MONDO:0008319 - protoporphyria, erythropoietic, 1

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MONDO:0011301 - pseudohypoparathyroidism type 1B

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MONDO:0014686 - short stature, microcephaly, and endocrine dysfunction

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MONDO:0008566 - thyroid cancer, nonmedullary, 2

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MONDO:0013771 - transient infantile hypertriglyceridemia and hepatosteatosis

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MONDO:0005148 - type 2 diabetes mellitus

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MONDO:0008297 - variegate porphyria

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MONDO:0957577 - variegate porphyria, childhood-onset

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MONDO:0010420 - X-linked erythropoietic protoporphyria

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