Abnormality of the cranial nerves
Symptom Information:
Symptom ID: | HPO:0001291 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||
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: |
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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) |