Cranial nerve paralysis
Symptom Information:
Symptom ID: | HPO:0006824 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |