Pulmonary hypoplasia

Symptom Information:

Symptom ID: HPO:0002089
Synonyms:
Hypoplastic lung [HPO:0002089]
Hypoplastic lungs [HPO:0002089]
Lung hypoplasia [HPO:0002089]
Congenital hypoplasia of lung (disorder) [Orphanet:32360]
Congenital hypoplasia of lung [Orphanet:32360]
Hypoplastic lung [OMIM:Hypoplastic lung]
Hypoplastic lungs [OMIM:Hypoplastic lungs]
Lung hypoplasia [OMIM:Lung hypoplasia]
Pulmonary hypoplasia [OMIM:Pulmonary hypoplasia]
Hypoplastic lungs/pulmonary hypoplasia/agenesis [Orphanet:32360]
Pulmonary hypoplasia [Orphanet:32360]
Pulmonary hypoplasia [MedDRA:10037407]
Agenesis, hypoplasia, and dysplasia of lung, congenital [MedDRA:10037407]
Lung hypoplasia (secondary to oligohydramnios) [OMIM:Lung hypoplasia (secondary to oligohydramnios)]
Quality:
Cross references:
Orphanet:32360 "Hypoplastic lungs/pulmonary hypoplasia/agenesis" [Orphanet:32360]
OMIM: "Hypoplastic lung" [OMIM:Hypoplastic lung]
OMIM: "Hypoplastic lungs" [OMIM:Hypoplastic lungs]
OMIM: "Lung hypoplasia" [OMIM:Lung hypoplasia]
OMIM: "Pulmonary hypoplasia" [OMIM:Pulmonary hypoplasia]
OMIM: "Lung hypoplasia (secondary to oligohydramnios)" [OMIM:Lung hypoplasia (secondary to oligohydramnios)]
UMLS:C0265783 "Congenital hypoplasia of lung" [Orphanet:32360]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the lungs
Orphanet Abnormality of the diaphragm
MedDRA Pulmonary and bronchial disorders congenital
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)
                   Pulmonary hypoplasia(HPO:0002089)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Respiratory disorders congenital(MedDRA:10038686)
       Pulmonary and bronchial disorders congenital(MedDRA:10025039)
          Pulmonary hypoplasia(HPO:0002089)
Database Frequency: 80 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-mandibular syndrome (Orphanet:958)
Acrocephalopolydactyly (Orphanet:221054)
Adenylosuccinate lyase deficiency (Orphanet:46)
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis (Orphanet:1112)
Atelosteogenesis type II (Orphanet:56304)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Bilateral renal agenesis (Orphanet:1848)
CHILD syndrome (Orphanet:139)
Cantrell pentalogy (Orphanet:1335)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
Diabetic embryopathy (Orphanet:1926)
Diaphanospondylodysostosis (Orphanet:66637)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Familial primary pulmonary hypoplasia (Orphanet:2257)
Fetal Gaucher disease (Orphanet:85212)
Fetal akinesia deformation sequence (Orphanet:994)
Fraser syndrome (Orphanet:2052)
Fryns syndrome (Orphanet:2059)
Gaucher disease type 2 (Orphanet:77260)
Genitopatellar syndrome (Orphanet:85201)
Goldenhar syndrome (Orphanet:374)
Greenberg dysplasia (Orphanet:1426)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Infantile hypophosphatasia (Orphanet:247651)
Jeune syndrome (Orphanet:474)
Joubert syndrome 21 (OMIM:615636)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Lethal Larsen-like syndrome (Orphanet:2371)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal restrictive dermopathy (Orphanet:1662)
Lissencephaly type 3 - metacarpal bone dysplasia (Orphanet:86822)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MICROPHTHALMIA, SYNDROMIC 12 (OMIM:615524)
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 (OMIM:615228)
Marden-Walker syndrome (Orphanet:2461)
Matthew-Wood syndrome (Orphanet:2470)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 6 (OMIM:612284)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Neu-Laxova syndrome (Orphanet:2671)
Opitz G/BBB syndrome (Orphanet:2745)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Perinatal lethal hypophosphatasia (Orphanet:247623)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
RENAL HYPODYSPLASIA/APLASIA 2 (OMIM:615721)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 (OMIM:615415)
Renal tubular dysgenesis (Orphanet:3033)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
SPONDYLOSPINAL THORACIC DYSOSTOSIS (OMIM:601809)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)
Short-rib thoracic dysplasia 6 with or without polydactyly (OMIM:263520)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Stüve-Wiedemann syndrome (Orphanet:3206)
THYMIC APLASIA WITH FETAL DEATH (OMIM:274210)
Tetraamelia - multiple malformations (Orphanet:3301)
Tetrasomy 12p (Orphanet:884)
Ulbright-Hodes syndrome (Orphanet:3404)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)
Zellweger syndrome (Orphanet:912)