Feeding difficulties
Symptom Information:
Symptom ID: | HPO:0011968 | ||||||||||||||||||
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 abdomen(HPO:0001438) Abdominal symptom(HPO:0011458) Feeding difficulties(HPO:0011968) MedDRA: |
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Database Frequency: | 240 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2p21 microdeletion syndrome | (Orphanet:163693) |
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY | (OMIM:231530) |
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY | (OMIM:210200) |
3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA | (OMIM:616271) |
AICARDI-GOUTIERES SYNDROME 4 | (OMIM:610333) |
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME | (OMIM:615510) |
ALG11-CDG | (Orphanet:280071) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Arnold-Chiari malformation type II | (Orphanet:1136) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
BAINBRIDGE-ROPERS SYNDROME | (OMIM:615485) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Biotinidase deficiency | (Orphanet:79241) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, MKB type | (Orphanet:293707) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
Bloom syndrome | (Orphanet:125) |
Bohring-Opitz syndrome | (Orphanet:97297) |
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 | (OMIM:604377) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 15q11.2 DELETION SYNDROME | (OMIM:615656) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
COENZYME Q10 DEFICIENCY, PRIMARY, 3 | (OMIM:614652) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
COG4-CDG | (Orphanet:263501) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 | (OMIM:615595) |
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cerebro-facio-articular syndrome | (Orphanet:314679) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Citrullinemia type I | (Orphanet:247525) |
Classic maple syrup urine disease | (Orphanet:268145) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Combined oxidative phosphorylation deficiency type 23 | (ORPHA:444013) |
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 type 1A | (Orphanet:258) |
Congenital muscular dystrophy with intellectual disability and severe epilepsy | (Orphanet:329178) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Costello syndrome | (Orphanet:3071) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
D,L-2-hydroxyglutaric aciduria | (Orphanet:356978) |
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL | (OMIM:125800) |
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
Distal monosomy 3p | (Orphanet:1620) |
Dubowitz syndrome | (Orphanet:235) |
Dysmorphism - conductive hearing loss - heart defect | (Orphanet:289553) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 | (OMIM:615833) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 | (OMIM:616341) |
ESOPHAGITIS, EOSINOPHILIC, 1 | (OMIM:610247) |
ESOPHAGITIS, EOSINOPHILIC, 2 | (OMIM:613412) |
Emanuel syndrome | (Orphanet:96170) |
Encephalopathy due to prosaposin deficiency | (Orphanet:139406) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Fatal infantile lactic acidosis with methylmalonic aciduria | (Orphanet:17) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fatal multiple mitochondrial dysfunction syndrome | (Orphanet:289573) |
GCS1-CDG | (Orphanet:79330) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Gaucher disease type 2 | (Orphanet:77260) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME | (OMIM:236450) |
HYPERCHLORHIDROSIS, ISOLATED | (OMIM:143860) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
Haddad syndrome | (Orphanet:99803) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hawkinsinuria | (Orphanet:2118) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary sensory and autonomic neuropathy type 6 | (Orphanet:314381) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hurler syndrome | (Orphanet:93473) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome | (Orphanet:363611) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Joubert syndrome 2 | (OMIM:608091) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Leprechaunism | (Orphanet:508) |
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect | (Orphanet:330050) |
MEGDEL syndrome | (Orphanet:352328) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
MEIER-GORLIN SYNDROME 3 | (OMIM:613803) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 | (OMIM:614607) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 | (OMIM:614608) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 | (OMIM:615834) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 | (OMIM:616158) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 | (OMIM:616268) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9 | (OMIM:616111) |
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C | (OMIM:615501) |
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY | (OMIM:616095) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
MPDU1-CDG | (Orphanet:79323) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 | (OMIM:605711) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14 | (OMIM:615350) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 | (OMIM:615351) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616326) |
MYASTHENIC SYNDROME, CONGENITAL, 17 | (OMIM:616304) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616314) |
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL | (OMIM:616322) |
MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616323) |
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL | (OMIM:616324) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy | (Orphanet:255235) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Monosomy 22q13 | (Orphanet:48652) |
Mulibrey nanism | (Orphanet:2576) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA | (OMIM:201300) |
Native American myopathy | (Orphanet:168572) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency | (Orphanet:88639) |
Niemann-Pick disease type A | (Orphanet:77292) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8 | (OMIM:615085) |
Ondine syndrome | (Orphanet:661) |
PEHO syndrome | (Orphanet:2836) |
PEHO-like syndrome | (Orphanet:99807) |
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) | (OMIM:614882) |
PEROXISOME BIOGENESIS DISORDER 11B | (OMIM:614885) |
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) | (OMIM:614887) |
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) | (OMIM:614872) |
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY | (OMIM:602342) |
PMM2-CDG | (Orphanet:79318) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1A | (OMIM:607596) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C | (OMIM:616081) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A | (OMIM:277470) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B | (OMIM:612389) |
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM | (OMIM:614501) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Paramyotonia congenita of Von Eulenburg | (Orphanet:684) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Pelizaeus-Merzbacher-like due to HSPD1 mutation | (Orphanet:280288) |
Peters-plus syndrome | (Orphanet:709) |
Phosphoserine aminotransferase deficiency | (Orphanet:284417) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
Propionic acidemia | (Orphanet:35) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
RFT1-CDG | (Orphanet:244310) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
STT3A-CDG | (Orphanet:370921) |
STT3B-CDG | (Orphanet:370924) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Steinert myotonic dystrophy | (Orphanet:273) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
TEMPLE SYNDROME | (OMIM:616222) |
TMCO1 defect syndrome | (Orphanet:228407) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Thyroid hemiagenesis | (Orphanet:95719) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
VAN MALDERGEM SYNDROME 1 | (OMIM:601390) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
VERHEIJ SYNDROME | (OMIM:615583) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Williams syndrome | (Orphanet:904) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
[DEL] COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23 | (OMIM:616198) |