Cranial nerve paralysis

Symptom Information:

Symptom ID: HPO:0006824
Synonyms:
Cranial nerve palsies [HPO:0006824]
Cranial nerve palsy [HPO:0006824]
Cranial nerve paresis [HPO:0006824]
Cranial nerve palsy [Orphanet:43020]
Cranial nerve palsies [Orphanet:43020]
Cranial nerve palsies [OMIM:Cranial nerve palsies]
Cranial nerve palsy [OMIM:Cranial nerve palsy]
Cranial nerve paralysis [OMIM:Cranial nerve paralysis]
Cranial nerve paresis [OMIM:Cranial nerve paresis]
Cranial nerves palsy [Orphanet:43020]
Cranial nerve paralysis [Orphanet:43020]
Cranial nerve paralysis [MedDRA:10061908]
Paralysis of cranial nerve NOS [MedDRA:10061908]
Paresis cranial nerve [MedDRA:10061911]
Quality:
Cross references:
HPO:0010628 "Facial palsy" [Orphanet:43020]
Orphanet:43020 "Cranial nerves palsy" [Orphanet:43020]
OMIM: "Cranial nerve palsies" [OMIM:Cranial nerve palsies]
OMIM: "Cranial nerve palsy" [OMIM:Cranial nerve palsy]
OMIM: "Cranial nerve paralysis" [OMIM:Cranial nerve paralysis]
OMIM: "Cranial nerve paresis" [OMIM:Cranial nerve paresis]
UMLS:C0151311 "Cranial nerve palsies" [Orphanet:43020]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Cranial nerve disorders NEC
HPO         Abnormality of the cranial nerves
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormality of the cranial nerves(HPO:0001291)
                   Cranial nerve paralysis(HPO:0006824)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Cranial nerve disorders (excl neoplasms)(MedDRA:10011305)
       Cranial nerve disorders NEC(MedDRA:10011306)
          Cranial nerve paralysis(HPO:0006824)
Database Frequency: 81 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Adult intestinal botulism (Orphanet:178487)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alveolar echinococcosis (Orphanet:284)
Atypical teratoid tumor (Orphanet:99966)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Behçet disease (Orphanet:117)
Botulism (Orphanet:1267)
CADASIL (Orphanet:136)
CHARGE syndrome (Orphanet:138)
CRANIAL NERVES, CONGENITAL PARESIS OF (OMIM:218100)
CRANIAL NERVES, RECURRENT PARESIS OF (OMIM:218200)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Carney-Stratakis syndrome (Orphanet:97286)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Chédiak-Higashi syndrome (Orphanet:167)
Cystinosis (Orphanet:213)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Desminopathy (Orphanet:98909)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Fanconi anemia (Orphanet:84)
Foodborne botulism (Orphanet:228371)
Gaucher disease (Orphanet:355)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
Granulomatosis with polyangiitis (Orphanet:900)
Griscelli disease (Orphanet:381)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
HYPEROSTOSIS CORTICALIS GENERALISATA (OMIM:239100)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hereditary neuropathy with liability to pressure palsies (Orphanet:640)
Hereditary pheochromocytoma-paraganglioma (Orphanet:29072)
Hydatidosis (Orphanet:400)
Hyperostosis corticalis generalisata (Orphanet:3416)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Iatrogenic botulism (Orphanet:254509)
Infant botulism (Orphanet:178478)
Inhalational botulism (Orphanet:254504)
Intestinal botulism (Orphanet:178481)
Isolated Dandy-Walker malformation (Orphanet:217)
Kawasaki disease (Orphanet:2331)
Leigh syndrome (Orphanet:506)
Lyme disease (Orphanet:91546)
Maffucci syndrome (Orphanet:163634)
Malignant atrophic papulosis (Orphanet:679)
Melkersson-Rosenthal syndrome (Orphanet:2483)
Melorheostosis (Orphanet:2485)
Metachondromatosis (Orphanet:2499)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Moebius syndrome (Orphanet:570)
Muckle-Wells syndrome (Orphanet:575)
Multiple osteochondromas (Orphanet:321)
Myopathy and diabetes mellitus (Orphanet:2596)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurofibromatosis type 2 (Orphanet:637)
Neutral lipid storage disease (Orphanet:165)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
Osteopetrosis (Orphanet:2781)
PAGET DISEASE OF BONE (OMIM:602080)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 2 (OMIM:601650)
PARAGANGLIOMAS 3 (OMIM:605373)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
ROBERTS SYNDROME (OMIM:268300)
Relapsing polychondritis (Orphanet:728)
Rhabdoid tumor (Orphanet:69077)
Riboflavin transporter deficiency (Orphanet:97229)
Roberts syndrome (Orphanet:3103)
SAPHO syndrome (Orphanet:793)
Scleroderma (Orphanet:801)
Steinert myotonic dystrophy (Orphanet:273)
TRAPS syndrome (Orphanet:32960)
Townes-Brocks syndrome (Orphanet:857)
Toxin-mediated infectious botulism (Orphanet:230800)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
Wound botulism (Orphanet:178475)