Neonatal hypotonia
Symptom Information:
Symptom ID: | HPO:0001319 | |||||||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Abnormal muscle tone(HPO:0003808) Muscular hypotonia(HPO:0001252) Neonatal hypotonia(HPO:0001319) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle tone abnormalities(MedDRA:10028343) Neonatal hypotonia(HPO:0001319) |
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Database Frequency: | 101 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
1p36 deletion syndrome | (Orphanet:1606) |
2,4-@DIENOYL-CoA REDUCTASE 1, MITOCHONDRIAL | (OMIM:222745) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
ADENOSINE MONOPHOSPHATE DEAMINASE 1 | (OMIM:102770) |
AICA-ribosiduria | (Orphanet:250977) |
ALG11-CDG | (Orphanet:280071) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
BONE MARROW FAILURE SYNDROME 2 | (OMIM:615715) |
Beta-ureidopropionase deficiency | (Orphanet:65287) |
Bethlem myopathy | (Orphanet:610) |
Bifunctional enzyme deficiency | (Orphanet:300) |
COENZYME Q10 DEFICIENCY, PRIMARY, 3 | (OMIM:614652) |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 | (OMIM:615595) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Central core disease | (Orphanet:597) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Cohen syndrome | (Orphanet:193) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital muscular dystrophy with integrin alpha-7 deficiency | (Orphanet:34520) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
D-glyceric aciduria | (Orphanet:941) |
Early myoclonic encephalopathy | (Orphanet:1935) |
Emery-Nelson syndrome | (Orphanet:1927) |
FG SYNDROME 2 | (OMIM:300321) |
FG SYNDROME 4 | (OMIM:300422) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fetal Gaucher disease | (Orphanet:85212) |
GRACILE syndrome | (Orphanet:53693) |
German syndrome | (Orphanet:2077) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Hereditary sensory and autonomic neuropathy type 6 | (Orphanet:314381) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Joubert syndrome 2 | (OMIM:608091) |
LEOPARD SYNDROME 3 | (OMIM:613707) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 | (OMIM:615074) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42 | (OMIM:615802) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 | (OMIM:615824) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | (OMIM:616094) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET | (OMIM:609500) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Moderate multiminicore disease with hand involvement | (Orphanet:178145) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 5p | (Orphanet:281) |
Mucolipidosis type 2 | (Orphanet:576) |
Multiple sulfatase deficiency | (Orphanet:585) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | (Orphanet:457185) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Oculocerebrorenal syndrome | (Orphanet:534) |
PEROXISOME BIOGENESIS DISORDER 1B | (OMIM:601539) |
PEROXISOME BIOGENESIS DISORDER 4B | (OMIM:614863) |
PEROXISOME BIOGENESIS DISORDER 5B | (OMIM:614867) |
PEROXISOME BIOGENESIS DISORDER 6B | (OMIM:614871) |
PEROXISOME BIOGENESIS DISORDER 7B | (OMIM:614873) |
PEROXISOME BIOGENESIS DISORDER 8B | (OMIM:614877) |
PLEOCONIAL MYOPATHY WITH SALT CRAVING | (OMIM:262900) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2E | (OMIM:615851) |
Paramyotonia congenita of Von Eulenburg | (Orphanet:684) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Polymicrogyria with optic nerve hypoplasia | (Orphanet:250972) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SOTOS SYNDROME 1 | (OMIM:117550) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Sotos syndrome | (Orphanet:821) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked non progressive cerebellar ataxia | (Orphanet:314978) |
X-linked progressive cerebellar ataxia | (Orphanet:1175) |