Hypothalamic hamartoma

Symptom Information:

Symptom ID: HPO:0002444
Synonyms:
Hypothalamic hamartoma [OMIM:Hypothalamic hamartoma]
Quality:
Cross references:
OMIM: "Hypothalamic hamartoma" [OMIM:Hypothalamic hamartoma]
Is a (Direct Parents):
HPO         Abnormal hypothalamus morphology
HPO         Cerebral hamartomata
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Neoplasm of the central nervous system(HPO:0100006)
                   Benign neoplasm of the central nervous system(HPO:0100835)
                      Cerebral hamartomata(HPO:0009731)
                         Hypothalamic hamartoma(HPO:0002444)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the central nervous system(HPO:0100006)
                Benign neoplasm of the central nervous system(HPO:0100835)
                   Cerebral hamartomata(HPO:0009731)
                      Hypothalamic hamartoma(HPO:0002444)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the central nervous system(HPO:0100006)
                   Benign neoplasm of the central nervous system(HPO:0100835)
                      Cerebral hamartomata(HPO:0009731)
                         Hypothalamic hamartoma(HPO:0002444)
          Neoplasm by histology(HPO:0011792)
             Hamartoma(HPO:0010566)
                Cerebral hamartomata(HPO:0009731)
                   Hypothalamic hamartoma(HPO:0002444)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Pallister-Hall syndrome (Orphanet:672)