Paraganglioma

Symptom Information:

Symptom ID: HPO:0002668
Synonyms:
Carotid body tumors [HPO:0002668]
Chemodectoma [HPO:0002668]
Chemodectomas [HPO:0002668]
Paragangliomas [HPO:0002668]
Gangliocytic paraganglioma (disorder) [Orphanet:50660]
Gangliocytic paraganglioma (morphologic abnormality) [Orphanet:50660]
Neoplasm of paraganglion (disorder) [Orphanet:50660]
Paraganglioma (disorder) [Orphanet:50660]
Paraganglioma (morphologic abnormality) [Orphanet:50660]
chemodectomas [HPO:0002668]
Paraganglioma [Orphanet:50660]
Carotid body tumors [OMIM:Carotid body tumors]
Chemodectomas [OMIM:Chemodectomas]
Paraganglioma [OMIM:Paraganglioma]
Paragangliomas [OMIM:Paragangliomas]
Pheochromocytoma/paraganglioma [Orphanet:50660]
Paraganglion neoplasm [Orphanet:50660]
Paraganglion neoplasm [MedDRA:10061332]
Neoplasm of uncertain behavior of paraganglia [MedDRA:10061332]
Neoplasm of uncertain behaviour of paraganglia [MedDRA:10061332]
Paraganglion neoplasm NOS [MedDRA:10061332]
Paraganglioma [MedDRA:10061332]
Carotid body tumors (most common location) [OMIM:Carotid body tumors (most common location)]
Carotid body tumors (most common) [OMIM:Carotid body tumors (most common)]
Chemodectoma [MedDRA:10051227]
Quality:
Cross references:
Orphanet:50660 "Pheochromocytoma/paraganglioma" [Orphanet:50660]
OMIM: "Carotid body tumors" [OMIM:Carotid body tumors]
OMIM: "Chemodectomas" [OMIM:Chemodectomas]
OMIM: "Paraganglioma" [OMIM:Paraganglioma]
OMIM: "Paragangliomas" [OMIM:Paragangliomas]
OMIM: "Carotid body tumors (most common location)" [OMIM:Carotid body tumors (most common location)]
OMIM: "Carotid body tumors (most common)" [OMIM:Carotid body tumors (most common)]
UMLS:C0030421 "chemodectomas" [HPO:0002668]
UMLS:C0030421 "Paraganglioma" [Orphanet:50660]
Is a (Direct Parents):
Orphanet Pheochromocytoma
Orphanet Neoplasm of the adrenal gland
MedDRA Paraendocrine neoplasms NEC
HPO         Neuroendocrine neoplasm
HPO         Chemodectoma
MedDRA Neoplasms benign site unspecified NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Neuroendocrine neoplasm(HPO:0100634)
                      Paraganglioma(HPO:0002668)
             Neoplasm of the endocrine system(HPO:0100568)
                Neuroendocrine neoplasm(HPO:0100634)
                   Paraganglioma(HPO:0002668)
       Abnormality of the endocrine system(HPO:0000818)
          Neoplasm of the endocrine system(HPO:0100568)
             Neuroendocrine neoplasm(HPO:0100634)
                Paraganglioma(HPO:0002668)
       Abnormality of the nervous system(HPO:0000707)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the peripheral nervous system(HPO:0100007)
                Neuroendocrine neoplasm(HPO:0100634)
                   Paraganglioma(HPO:0002668)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Neuroendocrine neoplasm(HPO:0100634)
                      Paraganglioma(HPO:0002668)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Neoplastic and ectopic endocrinopathies(MedDRA:10029112)
       Paraendocrine neoplasms NEC(MedDRA:10033773)
          Paraganglioma(HPO:0002668)
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Miscellaneous and site unspecified neoplasms benign(MedDRA:10027656)
       Neoplasms benign site unspecified NEC(MedDRA:10029106)
          Paraganglioma(HPO:0002668)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Carney-Stratakis syndrome (Orphanet:97286)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 2 (OMIM:601650)
PARAGANGLIOMAS 3 (OMIM:605373)
PARAGANGLIOMAS 4 (OMIM:115310)
PARAGANGLIOMAS 5 (OMIM:614165)
Von Hippel-Lindau disease (Orphanet:892)