Cryptophthalmos

Symptom Information:

Symptom ID: HPO:0001126
Synonyms:
Cryptophthalmos (disorder) [Orphanet:7050]
Cryptophthalmos [Orphanet:7050]
Cryptophthalmos [OMIM:Cryptophthalmos]
Cryptophthalmia/ankyloblepharon/synblepharon [Orphanet:7050]
Cryptophthalmos [MedDRA:10011497]
Quality:
Cross references:
Orphanet:7050 "Cryptophthalmia/ankyloblepharon/synblepharon" [Orphanet:7050]
OMIM: "Cryptophthalmos" [OMIM:Cryptophthalmos]
UMLS:C0311249 "Cryptophthalmos" [HPO:0001126]
UMLS:C0311249 "Cryptophthalmos" [Orphanet:7050]
Is a (Direct Parents):
HPO         Abnormality of globe size
HPO         Abnormality of globe location
MedDRA Ocular disorders congenital NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of globe location(HPO:0100886)
                      Cryptophthalmos(HPO:0001126)
                   Abnormality of globe size(HPO:0100887)
                      Cryptophthalmos(HPO:0001126)
                Abnormality of the orbital region(HPO:0000315)
                   Abnormality of globe location(HPO:0100886)
                      Cryptophthalmos(HPO:0001126)
                   Abnormality of globe size(HPO:0100887)
                      Cryptophthalmos(HPO:0001126)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of globe size(HPO:0100887)
                   Cryptophthalmos(HPO:0001126)
                Abnormality of globe location(HPO:0100886)
                   Cryptophthalmos(HPO:0001126)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Ocular disorders congenital NEC(MedDRA:10027673)
          Cryptophthalmos(HPO:0001126)
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Ablepharon macrostomia syndrome (Orphanet:920)
Fraser syndrome (Orphanet:2052)
Isolated cryptophthalmia (Orphanet:91396)