Pulmonary hypoplasia
Symptom Information:
Symptom ID: | HPO:0002089 | ||||||||||||||
Synonyms: |
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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) 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) |
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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) |