Congenital fibrosis of extraocular muscles

Symptom Information:

Symptom ID: HPO:0001491
Synonyms:
Congenital fibrosis of extraocular muscles (CFEOM) [HPO:0001491]
Congenital fibrosis of the extraocular muscles [HPO:0001491]
Congenital fibrosis of extraocular muscles [OMIM:Congenital fibrosis of extraocular muscles]
Congenital fibrosis of extraocular muscles (CFEOM) [OMIM:Congenital fibrosis of extraocular muscles (CFEOM)]
Congenital fibrosis of the extraocular muscles (1 family) [OMIM:Congenital fibrosis of the extraocular muscles (1 family)]
Congenital fibrosis of the extraocular muscles (9%) [OMIM:Congenital fibrosis of the extraocular muscles (9%)]
Congenital fibrosis of the extraocular muscles (CFEOM) [OMIM:Congenital fibrosis of the extraocular muscles (CFEOM)]
Quality:
Cross references:
OMIM: "Congenital fibrosis of extraocular muscles" [OMIM:Congenital fibrosis of extraocular muscles]
OMIM: "Congenital fibrosis of extraocular muscles (CFEOM)" [OMIM:Congenital fibrosis of extraocular muscles (CFEOM)]
OMIM: "Congenital fibrosis of the extraocular muscles (1 family)" [OMIM:Congenital fibrosis of the extraocular muscles (1 family)]
OMIM: "Congenital fibrosis of the extraocular muscles (9%)" [OMIM:Congenital fibrosis of the extraocular muscles (9%)]
OMIM: "Congenital fibrosis of the extraocular muscles (CFEOM)" [OMIM:Congenital fibrosis of the extraocular muscles (CFEOM)]
Is a (Direct Parents):
HPO         Abnormality of the extraocular muscles
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the extraocular muscles(HPO:0008049)
                Congenital fibrosis of extraocular muscles(HPO:0001491)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Bilateral frontal polymicrogyria (Orphanet:208444)
Congenital fibrosis of extraocular muscles (Orphanet:45358)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1 (OMIM:135700)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2 (OMIM:602078)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C (OMIM:609384)
Moebius syndrome (Orphanet:570)
Polymicrogyria due to TUBB2B mutation (Orphanet:300573)
TUKEL SYNDROME (OMIM:609428)