Bilateral microphthalmos

Symptom Information:

Symptom ID: HPO:0007633
Synonyms:
Microphthalmia, bilateral [HPO:0007633]
Bilateral microphthalmos [OMIM:Bilateral microphthalmos]
Microphthalmia, bilateral [OMIM:Microphthalmia, bilateral]
Microphthalmia, bilateral (isolated feature in some patients) [OMIM:Microphthalmia, bilateral (isolated feature in some patients)]
Quality:
Cross references:
OMIM: "Bilateral microphthalmos" [OMIM:Bilateral microphthalmos]
OMIM: "Microphthalmia, bilateral" [OMIM:Microphthalmia, bilateral]
OMIM: "Microphthalmia, bilateral (isolated feature in some patients)" [OMIM:Microphthalmia, bilateral (isolated feature in some patients)]
Is a (Direct Parents):
HPO         Microphthalmia
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 size(HPO:0100887)
                      Microphthalmia(HPO:0000568)
                         Bilateral microphthalmos(HPO:0007633)
                Abnormality of the orbital region(HPO:0000315)
                   Abnormality of globe size(HPO:0100887)
                      Microphthalmia(HPO:0000568)
                         Bilateral microphthalmos(HPO:0007633)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Microphthalmia(HPO:0000568)
                      Bilateral microphthalmos(HPO:0007633)
                Abnormality of globe size(HPO:0100887)
                   Microphthalmia(HPO:0000568)
                      Bilateral microphthalmos(HPO:0007633)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
Disorder of sex development - intellectual deficit (Orphanet:2983)
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE (OMIM:608763)
Fraser syndrome (Orphanet:2052)
HOLOPROSENCEPHALY 7 (OMIM:610828)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (OMIM:611638)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 (OMIM:613703)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Matthew-Wood syndrome (Orphanet:2470)
NANOPHTHALMOS 1 (OMIM:600165)
Nanophthalmia (Orphanet:35612)
Treacher-Collins syndrome (Orphanet:861)