Large sella turcica
Symptom Information:
Symptom ID: | HPO:0002690 | |||||
Synonyms: |
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Is a (Direct Parents): |
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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 skull(HPO:0000929) Abnormality of the sella turcica(HPO:0002679) Large sella turcica(HPO:0002690) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of the sella turcica(HPO:0002679) Large sella turcica(HPO:0002690) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
AMENORRHEA-GALACTORRHEA SYNDROME | (OMIM:104600) |
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES | (OMIM:109120) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Hurler syndrome | (Orphanet:93473) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
PITUITARY DWARFISM WITH LARGE SELLA TURCICA | (OMIM:262710) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |