Abnormality of the cranial nerves

Symptom Information:

Symptom ID: HPO:0001291
Synonyms:
Cranial nerve abnormality [HPO:0001291]
Cranial nerve disease [HPO:0001291]
Cranial nerve involvement [HPO:0001291]
Cranial nerve anomaly [Orphanet:42870]
Cranial nerve abnormality [OMIM:Cranial nerve abnormality]
Cranial nerve involvement [OMIM:Cranial nerve involvement]
Cranial nerve anomalies [Orphanet:42870]
Cranial nerve anomalies [OMIM:Cranial nerve anomalies]
Quality:
Cross references:
Orphanet:42870 "Cranial nerve anomalies" [Orphanet:42870]
OMIM: "Cranial nerve abnormality" [OMIM:Cranial nerve abnormality]
OMIM: "Cranial nerve involvement" [OMIM:Cranial nerve involvement]
OMIM: "Cranial nerve anomalies" [OMIM:Cranial nerve anomalies]
Is a (Direct Parents):
HPO         Abnormality of great auricular nerve
HPO         Abnormality of inferior alveolar nerve
HPO         Morphological abnormality of the central nervous system
Orphanet Structural anomalies of the nervous system
HPO         Abnormality of lingual nerve
HPO         Abnormality of infra-orbital nerve
HPO         Abnormality of glossopharyngeal nerve
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)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

8q12 microduplication syndrome (Orphanet:228399)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Argininemia (Orphanet:90)
Arnold-Chiari malformation type I (Orphanet:268882)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Blau syndrome (Orphanet:90340)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
CHARGE syndrome (Orphanet:138)
CHILD syndrome (Orphanet:139)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)
Charcot-Marie-Tooth disease type 4E (Orphanet:99951)
Craniometaphyseal dysplasia (Orphanet:1522)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Dysosteosclerosis (Orphanet:1782)
Familial multiple nevi flammei (Orphanet:624)
Familial primary localized cutaneous amyloidosis (Orphanet:353220)
Hypoglossia - hypodactyly (Orphanet:989)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Neutral lipid storage disease (Orphanet:165)
OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA (OMIM:258470)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Osteopetrosis (Orphanet:2781)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Syringomyelia (Orphanet:3280)
Worster-Drought syndrome (Orphanet:3465)