Aplasia/Hypoplasia of the lungs
Symptom Information:
| Symptom ID: | HPO:0006703 | ||
| 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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Aplasia/Hypoplasia of the lungs(HPO:0006703) MedDRA: |
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| Database Frequency: | 79 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Achondrogenesis | (Orphanet:932) |
| Achondrogenesis type 1A | (Orphanet:93299) |
| Achondrogenesis type 1B | (Orphanet:93298) |
| Achondrogenesis type 2 | (Orphanet:93296) |
| Acro-renal-mandibular syndrome | (Orphanet:958) |
| Acrocephalosyndactyly | (Orphanet:946) |
| Amniotic bands | (Orphanet:1034) |
| Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
| Arthrogryposis multiplex congenita | (Orphanet:1037) |
| Autosomal recessive amelia | (Orphanet:1027) |
| Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
| Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
| Bilateral renal agenesis | (Orphanet:1848) |
| Boomerang dysplasia | (Orphanet:1263) |
| CHILD syndrome | (Orphanet:139) |
| Campomelia, Cumming type | (Orphanet:1318) |
| Cantrell pentalogy | (Orphanet:1335) |
| Caudal regression sequence | (Orphanet:3027) |
| Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
| Congenital unilateral pulmonary hypoplasia | (Orphanet:2258) |
| Craniomicromelic syndrome | (Orphanet:1524) |
| Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
| Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
| Dysplastic cortical hyperostosis | (Orphanet:2204) |
| Ellis Van Creveld syndrome | (Orphanet:289) |
| Eye defects - arachnodactyly - cardiopathy | (Orphanet:2725) |
| Familial primary pulmonary hypoplasia | (Orphanet:2257) |
| Fetal akinesia deformation sequence | (Orphanet:994) |
| Focal dermal hypoplasia | (Orphanet:2092) |
| Fraser syndrome | (Orphanet:2052) |
| Fryns syndrome | (Orphanet:2059) |
| Genitopatellar syndrome | (Orphanet:85201) |
| Goldenhar syndrome | (Orphanet:374) |
| Growth delay - hydrocephaly - lung hypoplasia | (Orphanet:3035) |
| Holoprosencephaly | (Orphanet:2162) |
| Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
| Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
| Jeune syndrome | (Orphanet:474) |
| Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
| Lethal Larsen-like syndrome | (Orphanet:2371) |
| Lethal chondrodysplasia, Moerman type | (Orphanet:1420) |
| Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
| Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
| Lethal multiple pterygium syndrome | (Orphanet:33108) |
| Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
| Lethal recessive chondrodysplasia | (Orphanet:1423) |
| Lethal restrictive dermopathy | (Orphanet:1662) |
| Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
| Matthew-Wood syndrome | (Orphanet:2470) |
| Meacham syndrome | (Orphanet:3097) |
| Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
| Metatropic dysplasia | (Orphanet:2635) |
| Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
| NPHP3-related Meckel-like syndrome | (Orphanet:3032) |
| Neu-Laxova syndrome | (Orphanet:2671) |
| Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
| Orofaciodigital syndrome type 4 | (Orphanet:2753) |
| Osteocraniostenosis | (Orphanet:2763) |
| Otopalatodigital syndrome type 2 | (Orphanet:90652) |
| PAGOD syndrome | (Orphanet:991) |
| Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
| Prune belly syndrome | (Orphanet:2970) |
| Renal tubular dysgenesis | (Orphanet:3033) |
| Short rib-polydactyly syndrome | (Orphanet:1505) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
| Tetraamelia - multiple malformations | (Orphanet:3301) |
| Tetraploidy | (Orphanet:3305) |
| Thanatophoric dysplasia | (Orphanet:2655) |
| Thanatophoric dysplasia type 1 | (Orphanet:1860) |
| Thanatophoric dysplasia type 2 | (Orphanet:93274) |
| Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
| Tracheal agenesis | (Orphanet:3346) |
| Ulbright-Hodes syndrome | (Orphanet:3404) |
| VACTERL with hydrocephalus | (Orphanet:3412) |
| VACTERL/VATER association | (Orphanet:887) |
| Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
| Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
| Wolf-Hirschhorn syndrome | (Orphanet:280) |