Feeding difficulties in infancy
Symptom Information:
Symptom ID: | HPO:0008872 | ||
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) Feeding difficulties in infancy(HPO:0008872) MedDRA: |
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Database Frequency: | 153 / 7739 | ||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
48,XXYY syndrome | (Orphanet:10) |
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AICARDI-GOUTIERES SYNDROME 5 | (OMIM:612952) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Angelman syndrome | (Orphanet:72) |
Argininosuccinic aciduria | (Orphanet:23) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Atrial tachyarrhythmia with short PR interval | (Orphanet:844) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
BOWEN SYNDROME OF MULTIPLE MALFORMATIONS | (OMIM:211200) |
Barth syndrome | (Orphanet:111) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Biotinidase deficiency | (Orphanet:79241) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
COLD-INDUCED SWEATING SYNDROME 2 | (OMIM:610313) |
CORNELIA DE LANGE SYNDROME 3 | (OMIM:610759) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine uptake deficiency | (Orphanet:158) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Classic maple syrup urine disease | (Orphanet:268145) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital short bowel syndrome | (Orphanet:2301) |
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
Dihydropyrimidinuria | (Orphanet:38874) |
Dubowitz syndrome | (Orphanet:235) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
FG SYNDROME 4 | (OMIM:300422) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypoaldosteronism | (Orphanet:427) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Fatal infantile cytochrome C oxidase deficiency | (Orphanet:1561) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
GCS1-CDG | (Orphanet:79330) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease type 2 | (Orphanet:77260) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME | (OMIM:236450) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency | (Orphanet:71212) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Infantile hypophosphatasia | (Orphanet:247651) |
Intellectual deficit, Birk-Barel type | (Orphanet:166108) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated Pierre Robin syndrome | (Orphanet:718) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Joubert syndrome 10 | (OMIM:300804) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Kabuki syndrome | (Orphanet:2322) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Leigh syndrome | (Orphanet:506) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Menkes disease | (Orphanet:565) |
Methylcobalamin deficiency type cblG | (Orphanet:2170) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Moebius syndrome | (Orphanet:570) |
Monosomy 5p | (Orphanet:281) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NOONAN SYNDROME 7 | (OMIM:613706) |
Nemaline myopathy | (Orphanet:607) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Nephrogenic diabetes insipidus | (Orphanet:223) |
Niemann-Pick disease type A | (Orphanet:77292) |
Niemann-Pick disease type C | (Orphanet:646) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PEHO syndrome | (Orphanet:2836) |
PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER) | (OMIM:614859) |
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) | (OMIM:614862) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) | (OMIM:614870) |
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER) | (OMIM:614876) |
PMM2-CDG | (Orphanet:79318) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Pearson syndrome | (Orphanet:699) |
Pelizaeus-Merzbacher-like due to HSPD1 mutation | (Orphanet:280288) |
Peters-plus syndrome | (Orphanet:709) |
Phosphoserine aminotransferase deficiency | (Orphanet:284417) |
Pontocerebellar hypoplasia type 1 | (Orphanet:2254) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Propionic acidemia | (Orphanet:35) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Steinert myotonic dystrophy | (Orphanet:273) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Thyroid ectopia | (Orphanet:95712) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Williams syndrome | (Orphanet:904) |
Wolfram syndrome | (Orphanet:3463) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |