Single naris
Symptom Information:
Symptom ID: | HPO:0009932 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Abnormality of the nose(HPO:0000366) Abnormality of the nares(HPO:0005288) Single naris(HPO:0009932) MedDRA: |
||||
Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Holoprosencephaly | (Orphanet:2162) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism | (Orphanet:2250) |
Joubert syndrome 21 | (OMIM:615636) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
XK aprosencephaly | (Orphanet:3469) |