Protuberant abdomen

Symptom Information:

Symptom ID: HPO:0001538
Synonyms:
Abdominal protuberance [HPO:0001538]
Abdominal protuberance [OMIM:Abdominal protuberance]
Protuberant abdomen [OMIM:Protuberant abdomen]
Quality:
Cross references:
OMIM: "Abdominal protuberance" [OMIM:Abdominal protuberance]
OMIM: "Protuberant abdomen" [OMIM:Protuberant abdomen]
Is a (Direct Parents):
HPO         Abdominal distention
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abdominal symptom(HPO:0011458)
             Abdominal distention(HPO:0003270)
                Protuberant abdomen(HPO:0001538)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Cholesteryl ester storage disease (Orphanet:75234)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Diaphanospondylodysostosis (Orphanet:66637)
FIBROCHONDROGENESIS 1 (OMIM:228520)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Fibrochondrogenesis (Orphanet:2021)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Leprechaunism (Orphanet:508)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lysosomal acid lipase deficiency (Orphanet:275761)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Niemann-Pick disease type A (Orphanet:77292)
Opsismodysplasia (Orphanet:2746)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Rabson-Mendenhall syndrome (Orphanet:769)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Sialuria (Orphanet:3166)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Wolman disease (Orphanet:75233)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)