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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS


Term:endocrine system disease
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Accession:EFO:0001379 term browser browse the term
Definition:A disease involving the endocrine system. Any deviation from the normal structure or function of the endocrine system that is manifested by a characteristic set of symptoms and signs. Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES.
Synonyms:exact_synonym: DIS ENDOCRINE SYSTEM;   DOID:28;   Disease of endocrine gland;   Diseases of Endocrine System;   Disorder of endocrine gland;   Disorder of endocrine system;   Disorder of endocrine system (disorder);   ENDOCRINE DIS;   ENDOCRINE DISORDER NOS;   ENDOCRINE DISORDERS;   Endocrine Diseases;   Endocrine Diseases and Manifestations;   Endocrine System Diseases;   Endocrine System Disorder;   Endocrine disease;   Endocrine disorder;   Endocrine disorder NOS (disorder);   Endocrine disturbance;   Endocrine disturbance NOS;   Endocrine disturbance NOS (disorder);   Endocrine gland disease NOS;   Endocrine gland disease NOS (disorder);   Endocrinopathy;   Endocrinopathy, NOS;   Hormone abnormality;   Hormone abnormality (finding);   Hormone disorders;   Hormone disturbance;   Hormone disturbance NOS;   NCIT:C3009;   Unspecified endocrine disorder;   disease of endocrine system;   disease or disorder of endocrine system;   endocrine system disease or disorder;   http://identifiers.org/medgen/4043;   http://identifiers.org/mesh/D004700;   http://identifiers.org/snomedct/362969004;   http://linkedlifedata.com/resource/umls/id/C0014130;   thyroid or other glandular disorders
 xref: DOID:28;   ICD10:E34;   ICD9:259.8;   ICD9:259.9;   MEDGEN:4043;   MESH:D004700;   MONDO:0005151;   NANDO:1100009;   NANDO:2100109;   NCI:C27565;   NCI:C3009;   SCTID:362969004;   SNOMEDCT:362969004;   SNOMEDCT:84452004;   UMLS:C0014130
 external_ontology: disease_has_location EFO:UBERON:0000949;   in_taxon EFO:NCBITaxon:9606



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  experimental factor 0
    material property 0
      disposition 0
        disease 0
          endocrine system disease 0
            17,20-lyase deficiency, isolated 0
            17-alpha-hydroxylase/17,20-lyase deficiency, combined complete 0
            17-alpha-hydroxylase/17,20-lyase deficiency, combined partial 0
            Adamantinomatous Craniopharyngioma 0
            Bamforth-Lazarus syndrome 0
            Follicular Variant Thyroid Gland Papillary Carcinoma 0
            Genetic endocrine tumor + 0
            Leydig Cell Tumor + 0
            Leydig cell hypoplasia + 0
            Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 0
            NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction + 0
            Non-Neoplastic Bile Duct Disorder + 0
            Papillary Craniopharyngioma 0
            Papillary Tumor of the Pineal Region 0
            Poorly Differentiated Thyroid Gland Carcinoma + 0
            Rare genetic endocrine disease + 0
            Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 0
            Thyroid Gland Oncocytic Follicular Carcinoma 0
            Wolfram-like syndrome 0
            adrenal gland disease + 0
            autoimmune disorder of endocrine system + 0
            beta thalassemia + 0
            blepharophimosis - intellectual disability syndrome, SBBYS type 0
            campomelic dysplasia 0
            choledocholithiasis 0
            combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 0
            dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 0
            disorder of GNAS inactivation + 0
            disorders of vitamin D metabolism + 0
            duplication of the pituitary gland 0
            endocrine neoplasm + 0
            endocrine tuberculosis + 0
            familial hypocalciuric hypercalcemia + 0
            female athlete triad syndrome 0
            genito-palato-cardiac syndrome 0
            gonadal disorder + 0
            hereditary endocrine growth disease + 0
            hyperinsulinemic hypoglycemia + 0
            hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 0
            hypoinsulinemic hypoglycemia and body hemihypertrophy 0
            hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 0
            inherited obesity + 0
            liver disease + 0
            muscular pseudohypertrophy-hypothyroidism syndrome 0
            neuroendocrine disorder + 0
            pancreas disease + 0
            parathyroid disease + 0
            parneoplastic endocrine syndrome + 0
            pituitary deficiency + 0
            pituitary gland disease + 0
            polycystic ovary syndrome 0
            polyendocrinopathy + 0
            rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 0
            thymus gland disorder + 0
            thymus hyperplasia 0
            thyroid disease + 0
            thyroid hormone metabolism, abnormal + 0
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