Abnormal lung lobation
Symptom Information:
Symptom ID: | HPO:0002101 | ||||||
Synonyms: |
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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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Abnormal lung lobation(HPO:0002101) MedDRA: |
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Database Frequency: | 33 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Acalvaria | (Orphanet:945) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Bowen-Conradi syndrome | (Orphanet:1270) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Constriction rings syndrome | (Orphanet:295000) |
Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
Distal trisomy 14q | (Orphanet:1705) |
Distal trisomy 6p | (Orphanet:1745) |
FANCONI ANEMIA, COMPLEMENTATION GROUP B | (OMIM:300514) |
Fraser syndrome | (Orphanet:2052) |
Greenberg dysplasia | (Orphanet:1426) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hydrolethalus | (Orphanet:2189) |
Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
Ivemark syndrome | (Orphanet:97548) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
Matthew-Wood syndrome | (Orphanet:2470) |
Meacham syndrome | (Orphanet:3097) |
Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
Microcephaly - cardiac defect - lung malsegmentation | (Orphanet:2516) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Pallister-Hall syndrome | (Orphanet:672) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Terminal transverse defects of arm | (Orphanet:93937) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
Trisomy 13 | (Orphanet:3378) |