Incomplete partition of the cochlea type II

Symptom Information:

Symptom ID: HPO:0000376
Synonyms:
Mondini malformation [HPO:0000376]
Mondini malformation [OMIM:Mondini malformation]
Quality:
Cross references:
OMIM: "Mondini malformation" [OMIM:Mondini malformation]
Is a (Direct Parents):
HPO         Incomplete partition of the cochlea
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the inner ear(HPO:0000359)
             Morphological abnormality of the inner ear(HPO:0011390)
                Abnormality of cochlea(HPO:0000375)
                   Cochlear malformation(HPO:0008554)
                      Incomplete partition of the cochlea(HPO:0011373)
                         Incomplete partition of the cochlea type II(HPO:0000376)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

BOR syndrome (Orphanet:107)
BRANCHIOOTORENAL SYNDROME 1 (OMIM:113650)
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT (OMIM:600791)
Ear-patella-short stature syndrome (Orphanet:2554)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)