Abnormal lung lobation

Symptom Information:

Symptom ID: HPO:0002101
Synonyms:
Defective lung lobation [HPO:0002101]
Lung segmentation anomaly [Orphanet:32400]
Abnormal lung lobation [OMIM:Abnormal lung lobation]
Absent lobe/lung/segmentation defect/abnormal lobulation/sequestration [Orphanet:32400]
Abnormal lung lobation (in 1/4 patients) [OMIM:Abnormal lung lobation (in 1/4 patients)]
Lung lobe congenital absence [Orphanet:32400]
Quality:
Cross references:
HPO:0006525 "Lung segmentation defects" [Orphanet:32400]
Orphanet:32400 "Absent lobe/lung/segmentation defect/abnormal lobulation/sequestration" [Orphanet:32400]
OMIM: "Abnormal lung lobation" [OMIM:Abnormal lung lobation]
OMIM: "Abnormal lung lobation (in 1/4 patients)" [OMIM:Abnormal lung lobation (in 1/4 patients)]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
HPO         Abnormality of lung morphology
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:
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)