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encyclopedia of Rare Disease Annotation for Precision Medicine



   opitz g/bbb syndrome
  

Disease ID 1148
Disease opitz g/bbb syndrome
Definition
An X-linked syndrome caused by mutations in the MID1 gene or autosomal dominant syndrome caused by changes in chromosome 22. It is characterized by ocular hypertelorism, and defects of the larynx, trachea, or esophagus. Most males have hypospadias, cryptorchidism, underdeveloped scrotum, or a scrotum divided into two lobes. Mild intellectual disability and developmental delays occur in approximately half of the affected individuals.
Synonym
autosomal dominant opitz syndrome (ados)
bbb syndrome
chromosome 22q11.2 deletion syndrome, opitz phenotype
g syndrome
gbbb syndrome
gbbb2
hypertelorism hypospadias syndrome
hypertelorism with esophageal abnormalities and hypospadias
hypertelorism with esophageal abnormality and hypospadias
hypertelorism-hypospadias sydrome
hypertelorism-hypospadias syndrome
hypospadias-dysphagia syndrome
hypospadias-dysphagia, syndrome
ogs2
opitz bbb syndrome
opitz bbb-g syndrome
opitz bbbg syndrome
opitz g syndrome
opitz g-bbb syndrome
opitz gbbb syndrome, autosomal dominant
opitz gbbb syndrome, type ii
opitz oculogenitolaryngeal syndrome, type ii
opitz-frias syndrome
opitz-g syndrome, type 2
opitz-g syndrome, type ii
telecanthus with associated abnormalities
telecanthus-hypospadias syndrome
Orphanet
OMIM
DOID
UMLS
C1801950
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:152)
C0020598  |  hypoglycemia  |  5
C0011847  |  diabetes  |  4
C0019100  |  dengue hemorrhagic fever  |  3
C0020538  |  hypertension  |  3
C0032285  |  pneumonia  |  3
C0003125  |  anorexia nervosa  |  3
C0022658  |  renal disease  |  3
C0020598  |  hypoglycaemia  |  3
C0036420  |  localized scleroderma  |  2
C0003864  |  arthritis  |  2
C1621895  |  adrenal hyperplasia  |  2
C0017152  |  gastritis  |  2
C0025289  |  meningitis  |  2
C0014544  |  epilepsy  |  2
C0206667  |  adrenocortical adenoma  |  2
C0023787  |  lipodystrophy  |  2
C0022661  |  end-stage renal disease  |  2
C0013421  |  dystonia  |  2
C0026769  |  multiple sclerosis  |  2
C0004096  |  asthma  |  2
C0014038  |  encephalitis  |  2
C0022661  |  end stage renal disease  |  2
C0042870  |  vitamin d deficiency  |  2
C0442874  |  neuropathy  |  2
C0028754  |  obesity  |  2
C0042870  |  vitamin d defic  |  2
C0242379  |  lung cancer  |  1
C0001430  |  adenoma  |  1
C0026718  |  mucormycosis  |  1
C0041318  |  tuberculous meningitis  |  1
C1535927  |  charge syndrome  |  1
C0035258  |  restless legs  |  1
C1384514  |  primary aldosteronism  |  1
C0042961  |  volvulus  |  1
C0029001  |  onchocerciasis  |  1
C0039520  |  tenosynovitis  |  1
C0026846  |  muscle wasting  |  1
C0034065  |  pulmonary embolism  |  1
C0019294  |  inguinal hernias  |  1
C0013575  |  ectodermal dysplasia  |  1
C0018801  |  heart failure  |  1
C0003873  |  rheumatoid arthritis  |  1
C0024115  |  lung disease  |  1
C0003486  |  aortic aneurysm  |  1
C0019284  |  diaphragmatic hernia  |  1
C0024473  |  magnesium deficiency  |  1
C0276688  |  cryptococcal pneumonia  |  1
C0025202  |  melanoma  |  1
C0008924  |  cleft lip  |  1
C0238462  |  medullary thyroid carcinoma  |  1
C0679466  |  cognitive deficits  |  1
C0027765  |  nervous system disease  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0007682  |  central nervous system disease  |  1
C0011860  |  type 2 diabetes  |  1
C0021122  |  impulse control disorders  |  1
C0042164  |  uveitis  |  1
C0007682  |  central nervous system diseases  |  1
C0034150  |  purpura  |  1
C0086588  |  marasmus  |  1
C0030567  |  parkinson's disease  |  1
C0036439  |  scoliosis  |  1
C0022658  |  renal diseases  |  1
C0342494  |  adrenocortical hyperplasia  |  1
C0338591  |  transient global amnesia  |  1
C0007758  |  cerebellar ataxia  |  1
C0162429  |  malnutrition  |  1
C0026010  |  microphthalmos  |  1
C0020255  |  hydrocephalus  |  1
C0001206  |  acromegaly  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0014544  |  epileptic seizures  |  1
C0027765  |  nervous system diseases  |  1
C0007570  |  celiac disease  |  1
C0020459  |  hyperinsulinism  |  1
C0020224  |  polyhydramnios  |  1
C0025202  |  malignant melanoma  |  1
C0085278  |  antiphospholipid antibody syndrome  |  1
C0152020  |  gastroparesis  |  1
C0007786  |  brain ischemia  |  1
C0010068  |  coronary artery disease  |  1
C0022735  |  primary hypogonadism  |  1
C0013473  |  eating disorder  |  1
C0020619  |  hypogonadism  |  1
C0019937  |  horner syndrome  |  1
C0011884  |  diabetic retinopathy  |  1
C0006625  |  cachexia  |  1
C0022116  |  ischemia  |  1
C0020428  |  hyperaldosteronism  |  1
C0035078  |  kidney failure  |  1
C0040053  |  thrombosis  |  1
C0524851  |  neurodegenerative disease  |  1
C0266463  |  lissencephaly  |  1
C0032000  |  pituitary adenoma  |  1
C0085437  |  bacterial meningitis  |  1
C0023903  |  tumor of liver  |  1
C0206695  |  neuroendocrine carcinoma  |  1
C0014544  |  epileptic seizure  |  1
C0036992  |  short bowel syndrome  |  1
C0042165  |  anterior uveitis  |  1
C0206686  |  adrenocortical carcinoma  |  1
C0085541  |  frontal lobe epilepsy  |  1
C0267557  |  secretory diarrhea  |  1
C0030312  |  bone marrow failure  |  1
C0025309  |  meningoencephalitis  |  1
C0038012  |  spondylitis  |  1
C0003872  |  psoriatic arthritis  |  1
C0001621  |  adrenal disease  |  1
C0004509  |  azoospermia  |  1
C0020428  |  aldosteronism  |  1
C0007115  |  thyroid ca  |  1
C0027708  |  wilms tumor  |  1
C0409974  |  lupus erythematosus  |  1
C1704275  |  pyomyositis  |  1
C0149931  |  migraine  |  1
C0085436  |  cryptococcal meningitis  |  1
C0003857  |  arteriovenous malformation  |  1
C0026846  |  muscle atrophy  |  1
C0019294  |  inguinal hernia  |  1
C0751651  |  mitochondrial disorder  |  1
C0334684  |  renal adenoma  |  1
C0206667  |  adrenal adenoma  |  1
C0206667  |  adrenocortical adenomas  |  1
C0038013  |  ankylosing spondylitis  |  1
C0011991  |  diarrhea  |  1
C0549473  |  thyroid carcinoma  |  1
C0035309  |  retinopathy  |  1
C1868720  |  periventricular nodular heterotopia  |  1
C0406810  |  carney complex  |  1
C0271694  |  familial partial lipodystrophy  |  1
C0376545  |  hematologic malignancies  |  1
C0018378  |  guillain-barre syndrome  |  1
C0242379  |  lung cancers  |  1
C0034735  |  raynaud phenomenon  |  1
C0025362  |  mental retardation  |  1
C0376358  |  prostate cancer  |  1
C0011570  |  depression  |  1
C0011644  |  scleroderma  |  1
C0018799  |  heart disease  |  1
C0002418  |  amblyopia  |  1
C0158699  |  renal agenesis  |  1
C0015300  |  exophthalmos  |  1
C0235461  |  androgen excess  |  1
C0035258  |  restless legs syndrome  |  1
C0022806  |  kwashiorkor  |  1
C0015458  |  hemifacial atrophy  |  1
C0031511  |  pheochromocytoma  |  1
C0751651  |  mitochondrial disorders  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0235752  |  port-wine stain  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0152021  |  congenital heart disease  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
23384  |  SPECC1L  |  ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1148
Disease opitz g/bbb syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:23)
HP:0001263  |  Global developmental delay
HP:0005487  |  Prominent metopic ridge
HP:0000239  |  Large fontanelles
HP:0000600  |  Abnormality of the pharynx
HP:0000767  |  Pectus excavatum
HP:0000047  |  Hypospadias
HP:0000506  |  Telecanthus
HP:0000369  |  Low-set ears
HP:0000316  |  Hypertelorism
HP:0000668  |  Hypodontia
HP:0000407  |  Sensorineural hearing impairment
HP:0000494  |  Downslanted palpebral fissures
HP:0000286  |  Epicanthus
HP:0000175  |  Cleft palate
HP:0002093  |  Respiratory insufficiency
HP:0001608  |  Abnormality of the voice
HP:0000431  |  Wide nasal bridge
HP:0001249  |  Intellectual disability
HP:0000202  |  Oral cleft
HP:0000463  |  Anteverted nares
HP:0011220  |  Prominent forehead
HP:0000768  |  Pectus carinatum
HP:0011069  |  Increased number of teeth
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:158)
HP:0001943  |  Hypoglycemia  |  8
HP:0003774  |  End-stage renal failure  |  4
HP:0002039  |  Anorexia  |  4
HP:0002664  |  Neoplasia  |  4
HP:0002017  |  Nausea and vomiting  |  3
HP:0001249  |  Mental retardation  |  3
HP:0002090  |  Pneumonia  |  3
HP:0002148  |  Hypophosphataemia  |  3
HP:0001824  |  Weight loss  |  3
HP:0001369  |  Arthritis  |  3
HP:0001945  |  Fever  |  3
HP:0002013  |  Emesis  |  3
HP:0000822  |  Hypertension  |  3
HP:0000127  |  Salt wasting  |  3
HP:0030731  |  Carcinoma  |  3
HP:0002138  |  Subarachnoid hemorrhage  |  3
HP:0012531  |  Pain  |  3
HP:0001332  |  Dystonia  |  2
HP:0000365  |  Hearing impairment  |  2
HP:0002024  |  Intestinal malabsorption  |  2
HP:0012378  |  Fatigue  |  2
HP:0005263  |  Gastritis  |  2
HP:0002383  |  Encephalitis  |  2
HP:0001513  |  Obesity  |  2
HP:0100512  |  Vitamin D deficiency  |  2
HP:0002902  |  Hyponatremia  |  2
HP:0001287  |  Meningitis  |  2
HP:0008256  |  Adrenocortical adenomas  |  2
HP:0002527  |  Falls  |  2
HP:0012051  |  Low blood sugar after a meal  |  2
HP:0008221  |  Enlarged adrenal glands  |  2
HP:0000845  |  Acromegalic growth  |  2
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  2
HP:0002099  |  Asthma  |  2
HP:0009125  |  Lipodystrophy  |  2
HP:0011331  |  Atrophy of one side of the face  |  2
HP:0001339  |  Lissencephaly  |  1
HP:0000104  |  Renal agenesis  |  1
HP:0001336  |  Myoclonic jerks  |  1
HP:0000646  |  Wandering eyes  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0000815  |  Primary hypogonadism  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0007968  |  Persistent fetal vasculature  |  1
HP:0002487  |  Muscle spasms  |  1
HP:0002615  |  Low blood pressure  |  1
HP:0012452  |  Restless legs  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0002650  |  Scoliosis  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0000734  |  Disinhibition  |  1
HP:0001274  |  Absent corpus callosum  |  1
HP:0001662  |  Bradycardia  |  1
HP:0000027  |  Azoospermia  |  1
HP:0100257  |  Cleft hand  |  1
HP:0000519  |  Cataracts, lenticular, bilateral  |  1
HP:0010310  |  Chylothorax  |  1
HP:0002006  |  Tessier facial cleft  |  1
HP:0000997  |  Axillary freckling  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0001263  |  Developmental retardation  |  1
HP:0002390  |  Spinal arteriovenous malformation  |  1
HP:0000135  |  Hypogonadism  |  1
HP:0012432  |  Chronic fatigue  |  1
HP:0000716  |  Depression  |  1
HP:0100806  |  Sepsis  |  1
HP:0002019  |  Dyschezia  |  1
HP:0002861  |  Melanoma  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0001942  |  Metabolic acidosis  |  1
HP:0010828  |  Hemifacial spasm  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0001259  |  Coma  |  1
HP:0002637  |  Brain ischemia  |  1
HP:0004942  |  Aortic aneurysm  |  1
HP:0001052  |  port-wine stain  |  1
HP:0000776  |  Diaphragmatic hernia  |  1
HP:0002900  |  Hypokalemia  |  1
HP:0002865  |  Medullary thyroid carcinoma  |  1
HP:0002578  |  Gastroparesis  |  1
HP:0010534  |  Transient global amnesia  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0001010  |  Hypopigmentation of the skin  |  1
HP:0012721  |  Venous malformations  |  1
HP:0001289  |  Confusion  |  1
HP:0005528  |  Bone marrow hypoplasia  |  1
HP:0007260  |  Type II lissencephaly  |  1
HP:0000968  |  Ectodermal dysplasia  |  1
HP:0002608  |  Celiac disease  |  1
HP:0002580  |  Volvulus  |  1
HP:0002667  |  Wilms tumor  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0007033  |  Cerebellar dysplasia  |  1
HP:0000324  |  Asymmetry of face  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0001649  |  Tachycardia  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0000859  |  Mineralocorticoid excess  |  1
HP:0012122  |  Anterior uveitis  |  1
HP:0001250  |  Seizures  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0010783  |  Erythema  |  1
HP:0010864  |  Early and severe mental retardation  |  1
HP:0004395  |  Malnutrition  |  1
HP:0001251  |  Ataxia  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0006744  |  Adrenal carcinoma  |  1
HP:0000520  |  Anterior bulging of the globe of eye  |  1
HP:0000062  |  Ambiguous external genitalia  |  1
HP:0012049  |  Spasmodic dysphonia  |  1
HP:0004326  |  Cachexia  |  1
HP:0100822  |  Rectocele  |  1
HP:0000988  |  Exanthem  |  1
HP:0000825  |  Hyperinsulinaemic hypoglycaemia  |  1
HP:0000568  |  Abnormally small globe of eye  |  1
HP:0002153  |  Elevated serum potassium levels  |  1
HP:0003418  |  Back pain  |  1
HP:0040148  |  Cortical myoclonus  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0002277  |  Horner's syndrome  |  1
HP:0012165  |  Oligodactyly  |  1
HP:0001618  |  Dysphonia  |  1
HP:0100324  |  Progressive systemic scleroderma  |  1
HP:0002415  |  Degeneration of white matter of brain  |  1
HP:0003419  |  Low back pain  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0100790  |  Hernia  |  1
HP:0002014  |  Diarrhea  |  1
HP:0030880  |  Raynaud phenomenon  |  1
HP:0002321  |  Vertigo  |  1
HP:0011069  |  Extra teeth  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0002251  |  Hirschsprung megacolon  |  1
HP:0001548  |  Overgrowth  |  1
HP:0012054  |  Choroidal melanoma  |  1
HP:0000023  |  Inguinal hernia  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0000405  |  Conductive hearing loss  |  1
HP:0002018  |  Nausea  |  1
HP:0000122  |  Unilateral kidney agenesis  |  1
HP:0002304  |  Akinesia  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0000979  |  Purpura  |  1
HP:0002666  |  Pheochromocytoma  |  1
HP:0005208  |  Secretory diarrhea  |  1
HP:0002315  |  Headaches  |  1
HP:0007894  |  Retinal depigmentation  |  1
HP:0100022  |  Movement disorder  |  1
HP:0004322  |  Stature below 3rd percentile  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0000554  |  Uveitis  |  1
HP:0002020  |  Heartburn  |  1
HP:0100750  |  Pulmonary atelectasis  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0001480  |  Freckling  |  1
HP:0100615  |  Neoplasm of the ovary  |  1
Disease ID 1148
Disease opitz g/bbb syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Manually Genotypes:1)
Gene Mutation DOI Article Title
MID1-doi:10.1038/gim.2015.51Clinical performance of the CytoScan Dx Assay in diagnosing developmental delay/intellectual disability
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:8)
HP ID HP Name MP ID MP Name Annotation
HP:0000175Cleft palateMP:0013550abnormal secondary palate morphology
HP:0000431Wide nasal bridgeMP:0006292abnormal nasal placode morphologyany structural anomaly in the paired ectodermal placodes that come to lie in the bottom of the olfactory pits as the pits are deepened by the growth of the surrounding medial and lateral nasal processes; the nasal placode gives rise to the olfactory epith
HP:0001608Abnormality of the voiceMP:0013283failure of ventral body wall closurefailure of the lateral body wall folds (a combination of mesoderm and ectoderm arising on each side of the embryo) to progress ventrally and meet in the midline and/or fuse to close the ventral body wall; normally, this closure is aided by growth of the h
HP:0000202Oral cleftMP:0009890cleft secondary palatecongenital fissure of the tissues normally uniting to form the secondary palate
HP:0000407Sensorineural hearing impairmentMP:0006330syndromic hearing impairmenthearing impairment that is usually associated with malformations of the external ear and other inherited signs and symptoms
HP:0001263Global developmental delayMP:0002084abnormal developmental patterningabnormal systematic arrangement of the developing body along an axis
HP:0011069Increased number of teethMP:0020010decreased bone mineral density of femurreduction in the quatitative measurment value of mineral content of bone in the long bone of the thigh
HP:0000600Abnormality of the pharynxMP:0010732abnormal node of Ranvier morphologyany structural anomaly of the short unmyelinated segments of an axon between myelinated segments, where voltage gated channels accumulate and regenerate an action potential as it is conducted along the axon
Mapped by homologous gene(Total Items:23)
HP ID HP Name MP ID MP Name Annotation
HP:0000463Anteverted naresMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
HP:0000506TelecanthusMP:0020039increased bone ossificationincrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0000600Abnormality of the pharynxMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000316HypertelorismMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0000047HypospadiasMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0000407Sensorineural hearing impairmentMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0002093Respiratory insufficiencyMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000768Pectus carinatumMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000767Pectus excavatumMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0001263Global developmental delayMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0000175Cleft palateMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0001608Abnormality of the voiceMP:0020214susceptible to malignant hyperthermiaincreased susceptibility to hyperthermia triggered by exposure to certain drugs used for general anesthesia, specifically the volatile anesthetic agents and the neuromuscular blocking agent, succinylcholine
HP:0001249Intellectual disabilityMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0011220Prominent foreheadMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0000286EpicanthusMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000494Downslanted palpebral fissuresMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0000202Oral cleftMP:0014198absent pituitary infundibular stalkabsence of the apical portion of the tubular structure extending from the hypothalamus to the posterior lobe of the pituitary gland
HP:0005487Prominent metopic ridgeMP:0014125decreased amylin secretionreduction in the production or release of the polypeptide hormone that is normally co-secreted with insulin by the beta cells of the pancreatic islets of Langerhans and is known to inhibit glucagon secretion, delay gastric emptying, and act as a satiety a
HP:0000369Low-set earsMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0011069Increased number of teethMP:0020010decreased bone mineral density of femurreduction in the quatitative measurment value of mineral content of bone in the long bone of the thigh
HP:0000668HypodontiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000431Wide nasal bridgeMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000239Large fontanellesMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
Disease ID 1148
Disease opitz g/bbb syndrome
Case(Waiting for update.)