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 lingual nerve
Orphanet Structural anomalies of the nervous system
HPO         Morphological abnormality of the central nervous system
HPO         Abnormality of infra-orbital nerve
HPO         Abnormality of glossopharyngeal nerve
HPO         Abnormality of inferior alveolar nerve
HPO         Abnormality of great auricular 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)