Aplasia/Hypoplasia of the lungs

Symptom Information:

Symptom ID: HPO:0006703
Cross references:
Is a (Direct Parents):
HPO         Abnormality of lung morphology
Is a (Whole tree): HPO:
    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)
Database Frequency: 79 / 7739

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)