Large sella turcica

Symptom Information:

Symptom ID: HPO:0002690
Synonyms:
Enlarged sella turcica [HPO:0002690]
Prominent sella turcica [HPO:0002690]
Enlarged sella turcica [OMIM:Enlarged sella turcica]
Large sella turcica [OMIM:Large sella turcica]
Large sella turcica (rare) [OMIM:Large sella turcica (rare)]
Quality:
Cross references:
OMIM: "Enlarged sella turcica" [OMIM:Enlarged sella turcica]
OMIM: "Large sella turcica" [OMIM:Large sella turcica]
OMIM: "Large sella turcica (rare)" [OMIM:Large sella turcica (rare)]
Is a (Direct Parents):
HPO         Abnormality of the sella turcica
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       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)
MedDRA:
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)