Persistent pupillary membrane

Symptom Information:

Symptom ID: HPO:0009917
Synonyms:
Persistent pupillary membrane (1 patient, WWS) [OMIM:Persistent pupillary membrane (1 patient, WWS)]
Persistent pupillary membrane (in some patients) [OMIM:Persistent pupillary membrane (in some patients)]
Persistent pupillary membrane [MedDRA:10070872]
Quality:
Cross references:
OMIM: "Persistent pupillary membrane (1 patient, WWS)" [OMIM:Persistent pupillary membrane (1 patient, WWS)]
OMIM: "Persistent pupillary membrane (in some patients)" [OMIM:Persistent pupillary membrane (in some patients)]
Is a (Direct Parents):
MedDRA Congenital anterior segment disorders
HPO         Abnormality of the pupil
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 globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Abnormality of the pupil(HPO:0000615)
                         Persistent pupillary membrane(HPO:0009917)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Abnormality of the pupil(HPO:0000615)
                         Persistent pupillary membrane(HPO:0009917)
MedDRA:
Eye disorders(MedDRA:10015919)
    Congenital eye disorders (excl glaucoma)(MedDRA:10010463)
       Congenital anterior segment disorders(MedDRA:10010366)
          Persistent pupillary membrane(HPO:0009917)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Congenital blindness due to retinal non-attachment (Orphanet:300337)
ECTOPIA LENTIS ET PUPILLAE (OMIM:225200)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
PUPILLARY MEMBRANE, PERSISTENCE OF (OMIM:178900)
Proximal renal tubular acidosis (Orphanet:47159)