Protuberant abdomen
Symptom Information:
Symptom ID: | HPO:0001538 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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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 the abdomen(HPO:0001438) Abdominal symptom(HPO:0011458) Abdominal distention(HPO:0003270) Protuberant abdomen(HPO:0001538) MedDRA: |
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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) |